Data / Medical devices / Multi-Analyte Controls, All Kinds (Assayed)
Multi-Analyte Controls, All Kinds (Assayed) (JJY): 113 FDA-registered makers in 23 countries
113 establishments in 23 countries are registered with the FDA to make Multi-Analyte Controls, All Kinds (Assayed) (product code JJY, Class 1, 21 CFR 862.1660). 47 of them have a 510(k) clearance or PMA approval on file and 13 have a recall event. The FDA has issued 673 510(k) clearances under this code, the latest on March 31, 2017, and lists 60 recall events (0 Class I). FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Product code
- JJY
- Device class
- 1
- Regulation
- 862.1660
- Medical specialty
- Clinical Chemistry
Makers by country
| Country | Makers |
|---|---|
| United States | 62 |
| United Kingdom | 7 |
| Germany | 6 |
| Japan | 5 |
| Sweden | 4 |
| Ireland | 3 |
| France | 3 |
| South Korea | 3 |
| Canada | 2 |
| Netherlands | 2 |
| Norway | 2 |
| Taiwan | 2 |
| Poland | 2 |
| Denmark | 1 |
| Switzerland | 1 |
| Argentina | 1 |
| Spain | 1 |
| Hungary | 1 |
| China | 1 |
| Australia | 1 |
| Mexico | 1 |
| Israel | 1 |
| Italy | 1 |
Makers of Multi-Analyte Controls, All Kinds (Assayed)
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Bio-Rad Laboratories Inc. | Irvine, CA, United States | Manufacturer | 48 | January 10, 2017 | 0 | 1 | 0 | api.fda.gov |
| Bio-Rad Laboratories Inc. | Irvine, CA, United States | Manufacturer | 48 | January 10, 2017 | 0 | 0 | 0 | api.fda.gov |
| Cliniqa Corporation | San Marcos, CA, United States | Contract manufacturer, Manufacturer | 27 | January 23, 2012 | 0 | 0 | 0 | api.fda.gov |
| Randox Laboratories Limited | CRUMLIN, COUNTY ANTRIM Antrim and Newtownabbey, United Kingdom | Contract manufacturer, Manufacturer, Repackager or relabeler | 19 | December 8, 2014 | 0 | 0 | 0 | api.fda.gov |
| LGC Clinical Diagnostics, Inc. | Cumberland Foreside, ME, United States | Manufacturer | 9 | June 25, 2009 | 0 | 0 | 0 | api.fda.gov |
| Bionostics, Inc. | Devens, MA, United States | Contract manufacturer, Manufacturer | 7 | June 19, 2000 | 0 | 0 | 0 | api.fda.gov |
| Helena Laboratories, Corp. | Beaumont, TX, United States | Manufacturer | 7 | October 7, 2013 | 0 | 1 | 0 | api.fda.gov |
| Roche Diagnostics GMBH | MANNHEIM Baden-Wurttemberg, Germany | Exporter to the US, Manufacturer, Repackager or relabeler | 7 | September 1, 2010 | 0 | 0 | 0 | api.fda.gov |
| Beckman Coulter, Inc. | Brea, CA, United States | Specification developer | 6 | March 5, 2001 | 0 | 1 | 0 | api.fda.gov |
| DIAMOND DIAGNOSTICS Inc | Holliston, MA, United States | Manufacturer | 6 | April 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| Horiba Instruments Incorporated | Canton, MI, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 6 | April 11, 2007 | 0 | 3 | 0 | api.fda.gov |
| Nova Biomedical Corporation | Waltham, MA, United States | Complaint file establishment, Contract manufacturer, Manufacturer, Manufacturer for export, Specification developer | 6 | August 27, 2010 | 0 | 0 | 0 | api.fda.gov |
| Techno-Path Manufacturing Ltd. | Ballina Tipperary, Ireland | Complaint file establishment, Exporter to the US, Manufacturer, Repackager or relabeler | 5 | March 31, 2017 | 0 | 1 | 0 | api.fda.gov |
| Fisher Diagnostics | Middletown, VA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 4 | September 23, 2005 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Inc. | Tarrytown, NY, United States | Complaint file establishment, Specification developer | 4 | December 19, 2003 | 0 | 2 | 0 | api.fda.gov |
| Ortho-Clinical Diagnostics, Inc. | Rochester, NY, United States | Complaint file establishment, Specification developer | 3 | November 4, 1998 | 0 | 0 | 0 | api.fda.gov |
| Ortho-Clinical Diagnostics | Pencoed Bridgend, United Kingdom | Manufacturer | 3 | November 4, 1998 | 0 | 0 | 0 | api.fda.gov |
| Quantimetrix Corp. | Redondo Beach, CA, United States | Manufacturer | 3 | April 8, 1997 | 0 | 1 | 0 | api.fda.gov |
| Abbott Point Of Care Canada Limited | Ottawa Ontario, Canada | Specification developer | 2 | June 2, 2008 | 0 | 0 | 0 | api.fda.gov |
| Eurotrol B.V. | EDE Gelderland, Netherlands | Manufacturer | 2 | July 26, 2013 | 0 | 0 | 0 | api.fda.gov |
| Germaine Laboratories, Inc. | San Antonio, TX, United States | Manufacturer, Repackager or relabeler | 2 | September 17, 2008 | 0 | 0 | 0 | api.fda.gov |
| Kamiya Biomedical Company LLC | Tukwila, WA, United States | Manufacturer | 2 | September 29, 1998 | 0 | 0 | 0 | api.fda.gov |
| LGC Clinical Diagnostics, Inc. | Milford, MA, United States | Manufacturer | 2 | August 12, 1997 | 0 | 0 | 0 | api.fda.gov |
| Opti Medical Systems Inc. | Roswell, GA, United States | Manufacturer, Specification developer | 2 | June 19, 2000 | 0 | 0 | 0 | api.fda.gov |
| Phoenix Diagnostics, Inc. | Natick, MA, United States | Manufacturer | 2 | September 6, 1991 | 0 | 0 | 0 | api.fda.gov |
| Sebia | EVRY Essonne, France | Manufacturer | 2 | November 7, 2011 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Inc | East Walpole, MA, United States | Specification developer | 2 | April 8, 1997 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthcare Diagnostics Products GmbH | MARBURG Hesse, Germany | Manufacturer | 2 | June 10, 2002 | 0 | 0 | 0 | api.fda.gov |
| Teco Diagnostics | Anaheim, CA, United States | Manufacturer | 2 | October 4, 1994 | 0 | 0 | 0 | api.fda.gov |
| Utak Laboratories, Inc. | Valencia, CA, United States | Manufacturer | 2 | October 6, 1988 | 0 | 1 | 0 | api.fda.gov |
| VitalScientific | SEES Normandie, France | Manufacturer | 2 | September 14, 2011 | 0 | 0 | 0 | api.fda.gov |
| Alere San Diego, Inc. | San Diego, CA, United States | Specification developer | 1 | December 21, 2010 | 0 | 4 | 0 | api.fda.gov |
| Bialex Lab | Wichita Falls, TX, United States | Manufacturer | 1 | December 9, 2004 | 0 | 0 | 0 | api.fda.gov |
| Fujirebio Diagnostics AB | Molndal Vastra Gotaland, Sweden | Manufacturer | 1 | October 5, 2010 | 0 | 0 | 0 | api.fda.gov |
| Fujirebio Diagnostics, AB | Gothenburg Vastra Gotaland, Sweden | Manufacturer | 1 | October 5, 2010 | 0 | 0 | 0 | api.fda.gov |
| Hemagen Diagnostics, Inc. | Baltimore, MD, United States | Manufacturer | 1 | May 23, 1986 | 0 | 0 | 0 | api.fda.gov |
| More Diagnostics Inc. | Los Osos, CA, United States | Manufacturer | 1 | March 18, 2005 | 0 | 0 | 0 | api.fda.gov |
| Microgenics Corporation | Fremont, CA, United States | Contract manufacturer, Manufacturer, Manufacturer for export | 1 | December 21, 2001 | 0 | 6 | 0 | api.fda.gov |
| Polymer Technology Systems | Whitestown, IN, United States | Manufacturer | 1 | August 21, 2002 | 0 | 0 | 0 | api.fda.gov |
| Qualigen, Inc. | Carlsbad, CA, United States | Manufacturer | 1 | March 8, 2013 | 0 | 0 | 0 | api.fda.gov |
| Quidel Cardiovascular Inc. | San Diego, CA, United States | Manufacturer, Manufacturer for export | 1 | December 7, 2007 | 0 | 0 | 0 | api.fda.gov |
| Radiometer Medical Aps | BROENSHOEJ Hovedstaden, Denmark | Complaint file establishment, Manufacturer | 1 | October 12, 2005 | 0 | 0 | 0 | api.fda.gov |
| Randox Laboratories Limited | ANTRIM, COUNTY ANTRIM Antrim and Newtownabbey, United Kingdom | Contract manufacturer, Manufacturer, Repackager or relabeler | 1 | September 9, 2004 | 0 | 0 | 0 | api.fda.gov |
| Roche Diagnostics International Ltd. | ROTKREUZ Zug, Switzerland | Manufacturer, Repackager or relabeler | 1 | August 28, 2003 | 0 | 0 | 0 | api.fda.gov |
| Scantibodies Laboratory, Inc. | Santee, CA, United States | Manufacturer | 1 | February 14, 1996 | 0 | 0 | 0 | api.fda.gov |
| Stanbio Laboratory | Boerne, TX, United States | Manufacturer, Repackager or relabeler | 1 | September 25, 1995 | 0 | 0 | 0 | api.fda.gov |
| Wiener Laboratorios S.A.I.C. | ROSARIO Santa Fe, Argentina | Manufacturer | 1 | March 19, 2003 | 0 | 0 | 0 | api.fda.gov |
| Aalto Scientific Ltd. | Eatonton, GA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alfa Wassermann | West Caldwell, NJ, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ansh Labs, LLC | Webster, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Axiom Diagnostics, Inc. | Tampa, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Axis-Shield Diagnostics, Ltd. | DUNDEE Scotland, United Kingdom | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Abbott Diagnostics Technologies AS | Oslo, Norway | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Access Bio, Inc. | Monroe Township, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beckman Coulter, Inc. | Carlsbad, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bio-Rad Laboratories, Inc. | Woodinville, WA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biokit S.A. | LLISSA D AMUNT Barcelona, Spain | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioresource Technology | Weston, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Boditech Med Inc. | Chuncheon Gangwon, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beckman Coulter Ireland Inc | O CALLAGHANS MILLS Clare, Ireland | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bio-Rad Laboratories, Inc. | Hercules, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioptik Technology, Inc. | Jhunan Township Miaoli, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Chromsystems Instruments & Chemicals GMBH | Gräfelfing Bavaria, Germany | Manufacturer | 0 | 0 | 3 | 0 | api.fda.gov | |
| Cone Bioproducts Of Seguin LLC | Seguin, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Currier Plastics | Auburn, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Denka Co., Ltd. | GOSEN-SHI Niigata, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diasorin Inc. | Stillwater, MN, United States | Contract manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DRG Instruments GMBH | MARBURG Hesse, Germany | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diamond Diagnostics Inc. | Budapest, Hungary | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| ELITechGroup Inc | Logan, UT, United States | Contract manufacturer, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Eps Bio Technology Corp. | Hsinchu Hsinchu(County), Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Getein Biotech, Inc. | Nanjing Jiangsu, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gropep Bioreagents Pty Ltd | Adelaide South Australia, Australia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Horiba Abx SAS | MONTPELLIER Herault, France | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Horiba Ltd. | Kyoto, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| High Technology, Inc. | North Attleboro, MA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inflammatix | Sunnyvale, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inova Diagnostics, Inc. | San Diego, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Instrumentation Laboratory Co. | Bedford, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Instrumentation Laboratory Co. | Orangeburg, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laboratorios Scantibodies, S.A. de C.V. | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lumos Diagnostics, Inc. | Carlsbad, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medica Corp. | Bedford, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Monobind, Inc. | Lake Forest, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MeMed Diagnostics Ltd | Tirat Carmel Haifa, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nanoentek Inc | Hwaseong Gyeonggi, South Korea | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nanoentek Inc | Seoul, South Korea | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nittobo Medical Co., Ltd. Medical Development Center | Koriyama Fukushima, Japan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nova Biomedical Corporation Diabetes Products | Billerica, MA, United States | Complaint file establishment, Contract manufacturer, Manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nova Biomedical Corporation | Billerica, MA, United States | Contract manufacturer, Manufacturer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nypro Inc. (Chicago) | Gurnee, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ortho-Clinical Diagnostics, Inc. | Rochester, NY, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 1 | 0 | api.fda.gov | |
| Ortho-Clinical Diagnostics, Inc. | Rochester, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phadia AB | Uppsala, Sweden | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phadia AB | Uppsala, Sweden | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phadia GMBH | FREIBURG Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| R & D Systems, Inc. | Minneapolis, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Roche Diagnostics GMBH | PENZBERG Bavaria, Germany | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiometer Solutions Sp. z o.o. | Stargard Zachodniopomorskie, Poland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiometer Sp. z o.o | Stargard Zachodniopomorskie, Poland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sentinel CH. SPA | Milano, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sero AS | Billingstad Oslo, Norway | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Inc. | Newark, DE, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Products Limited | LLANBERIS Wales, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STS Corporation | Duluth, GA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sysmex Corporation | KOBE Hyogo, Japan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sysmex Corporation Techno Park | KOBE Hyogo, Japan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sekisui Diagnostics P.E.I. Inc. | CHARLOTTETOWN Prince Edward Island, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Binding Site | Kings Norton Birmingham, United Kingdom | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Binding Site Group Ltd. | Birmingham, United Kingdom | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Verax Biomedical Incorporated | Westborough, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| VitalScientific B.V. | SPANKEREN Gelderland, Netherlands | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Waters Technologies Ireland, Ltd. | DRINAGH Wexford, Ireland | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 31, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.