Skip to the page

Data / Medical devices / System, Irrigation, Urological

System, Irrigation, Urological (LJH): 28 FDA-registered makers in 9 countries

28 establishments in 9 countries are registered with the FDA to make System, Irrigation, Urological (product code LJH, Class 2, 21 CFR 876.5130). 15 of them have a 510(k) clearance or PMA approval on file and 2 have a recall event. The FDA has issued 30 510(k) clearances under this code, the latest on October 23, 2026, and lists 4 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
LJH
Device class
2
Regulation
876.5130
Medical specialty
Gastroenterology, Urology

Makers by country

CountryMakers
United States13
China4
Germany3
Dominican Republic2
Switzerland2
Costa Rica1
Malta1
Canada1
Honduras1

Makers of System, Irrigation, Urological

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
Karl Storz Endoscopy-America, Inc.Auburn, MA, United StatesContract manufacturer, Repackager or relabeler5July 7, 2017000api.fda.gov
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer3June 9, 1999000api.fda.gov
Amsino Medical (kunshan) Co., Ltd.KUNSHAN CITY Jiangsu, ChinaContract manufacturer, Manufacturer1December 19, 2007000api.fda.gov
Avid Medical, Inc. A Medical Action Ind. Company 305Toano, VA, United StatesManufacturer, Repackager or relabeler1March 10, 2003000api.fda.gov
B. Braun Medical Inc.Bethlehem, PA, United StatesSpecification developer1September 10, 2026000api.fda.gov
Baxter Healthcare CorporationRound Lake, IL, United StatesComplaint file establishment, Specification developer1May 14, 1996000api.fda.gov
Baxter Productos Medicos, Ltda.1-7052 Cartago, Costa RicaManufacturer1May 14, 1996000api.fda.gov
Baxter Healthcare, S.A.Haina San Cristobal, Dominican RepublicManufacturer1May 14, 1996000api.fda.gov
Baxter LimitedMarsa, MaltaSpecification developer1May 14, 1996000api.fda.gov
Canadian Hospital Specialties Ltd.OAKVILLE Ontario, CanadaManufacturer1November 28, 2001010api.fda.gov
DePuy Mitek, Inc.Raynham, MA, United StatesSpecification developer1May 8, 1998000api.fda.gov
Intl. Medsurg Connection, Inc.Schaumburg, IL, United StatesSpecification developer1March 10, 2003000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer1June 10, 1997000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesSpecification developer1October 25, 2004010api.fda.gov
Stryker Puerto Rico, LLC.Arroyo, PR, United StatesManufacturer1October 25, 2004000api.fda.gov
Auris Health, IncSanta Clara, CA, United StatesSpecification developer0000api.fda.gov
Auris Health, Inc.San Jose, CA, United StatesManufacturer0000api.fda.gov
B. Braun Dominican Republic Inc.SANTO DOMINGO Distrito Nacional, Dominican RepublicContract manufacturer0000api.fda.gov
B. Braun Us Device Manufacturing LLCAllentown, PA, United StatesContract manufacturer0000api.fda.gov
Changzhou DSB Medical Co., LtdChangzhou City Jiangsu, ChinaContract manufacturer0000api.fda.gov
Gcmedica Enterprise Ltd. (wuxi)Wuxi Jiangsu, ChinaContract manufacturer0000api.fda.gov
Gebruder Renggli, AGSchaffhausen, SwitzerlandContract manufacturer0000api.fda.gov
Honduras Kitting, S.A.Villanueva Cortes, HondurasContract manufacturer0000api.fda.gov
Jiangsu Shenli Medical Production Co.,ltdCHANGZHOU Jiangsu, ChinaContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Karl Storz Se & Co. KGNEUHAUSEN OBECK Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Nexus Medical, LLCLenexa, KS, United StatesContract manufacturer0000api.fda.gov
Storz Endoskop Produktions GMBHSchaffhausen, SwitzerlandContract manufacturer0000api.fda.gov

Updated October 23, 2026. 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.