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Data / Medical devices / Analyzer, Chemistry, Micro, For Clinical Use

Analyzer, Chemistry, Micro, For Clinical Use (JJF): 27 FDA-registered makers in 11 countries

27 establishments in 11 countries are registered with the FDA to make Analyzer, Chemistry, Micro, For Clinical Use (product code JJF, Class 1, 21 CFR 862.2170). 8 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 57 510(k) clearances under this code, the latest on March 31, 2006, and lists 10 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
JJF
Device class
1
Regulation
862.2170
Medical specialty
Clinical Chemistry

Makers by country

CountryMakers
United States9
Germany3
Switzerland3
China3
United Kingdom3
Italy1
India1
Japan1
Australia1
Finland1
Taiwan1

Makers of Analyzer, Chemistry, Micro, For Clinical Use

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Astoria-Pacific, Inc.Clackamas, OR, United StatesManufacturer2September 2, 1988000api.fda.gov
Roche Diagnostics GMBHMANNHEIM Baden-Wurttemberg, GermanyExporter to the US, Manufacturer2February 1, 2002000api.fda.gov
Roche Molecular Systems, Inc.Pleasanton, CA, United StatesSpecification developer2December 17, 2003000api.fda.gov
Beckman Coulter, Inc.Brea, CA, United StatesSpecification developer1December 31, 1986010api.fda.gov
DiaSorin Italia S.p.A.SALUGGIA Vercelli, ItalyManufacturer, Specification developer1March 31, 2006000api.fda.gov
Infrared Laboratory Systems dba SYNERMEDWestfield, IN, United StatesManufacturer1June 26, 1997000api.fda.gov
Roche Diagnostics International Ltd.ROTKREUZ Zug, SwitzerlandManufacturer1February 1, 2002000api.fda.gov
Siemens Healthcare Diagnostics Inc.Newark, DE, United StatesManufacturer1June 10, 1991000api.fda.gov
Accuster Technologies Pvt. Ltd.New Delhi, IndiaManufacturer0000api.fda.gov
Autobio Labtec Instruments Co., Ltd.Zhengzhou Henan, ChinaManufacturer0000api.fda.gov
Biochrom LtdCAMBRIDGE Cambridgeshire, United KingdomComplaint file establishment, Manufacturer0000api.fda.gov
Boston Easy Biotech IncBelmont, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Biochrom USHolliston, MA, United StatesContract manufacturer0000api.fda.gov
Diasorin Inc.Stillwater, MN, United StatesManufacturer0000api.fda.gov
DiaSorin Deutschland GmbHDietzenbach Hesse, GermanyContract manufacturer0000api.fda.gov
DiaSorin Italia S.p.A UK BranchDartford Kent, United KingdomContract manufacturer0000api.fda.gov
Furuno Electric Co., Ltd.NISHINOMIYA-CITY Hyogo, JapanManufacturer0000api.fda.gov
Getein Biotech, Inc.Nanjing Jiangsu, ChinaManufacturer0000api.fda.gov
Innovation Scientific Pty LtdVineyard New South Wales, AustraliaComplaint file establishment, Contract manufacturer0000api.fda.gov
Labsystems DiagnosticsVantaa Uusimaa, FinlandManufacturer0000api.fda.gov
Randox Laboratories LimitedCRUMLIN, COUNTY ANTRIM Antrim and Newtownabbey, United KingdomManufacturer0000api.fda.gov
Stratec SeBIRKENFELD, GRAEFENHAUSEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
STRATEC Switzerland AGBeringen Schaffhausen, SwitzerlandContract manufacturer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Tecan Schweiz AGMAENNEDORF ZUERICH Zurich, SwitzerlandManufacturer0000api.fda.gov
TST Biomedical Electronics Co., Ltd.Taoyuan, TaiwanExporter to the US, Specification developer0000api.fda.gov
Wuhan Landing Intelligence Medical Co.,LtdWuhan Hubei, ChinaManufacturer0000api.fda.gov

Updated March 31, 2006. 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.