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.
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- Product code
- LJH
- Device class
- 2
- Regulation
- 876.5130
- Medical specialty
- Gastroenterology, Urology
Makers by country
| Country | Makers |
|---|---|
| United States | 13 |
| China | 4 |
| Germany | 3 |
| Dominican Republic | 2 |
| Switzerland | 2 |
| Costa Rica | 1 |
| Malta | 1 |
| Canada | 1 |
| Honduras | 1 |
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.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Karl Storz Endoscopy-America, Inc. | Auburn, MA, United States | Contract manufacturer, Repackager or relabeler | 5 | July 7, 2017 | 0 | 0 | 0 | api.fda.gov |
| Karl Storz Se & Co KG | TUTTLINGEN Baden-Wurttemberg, Germany | Specification developer | 3 | June 9, 1999 | 0 | 0 | 0 | api.fda.gov |
| Amsino Medical (kunshan) Co., Ltd. | KUNSHAN CITY Jiangsu, China | Contract manufacturer, Manufacturer | 1 | December 19, 2007 | 0 | 0 | 0 | api.fda.gov |
| Avid Medical, Inc. A Medical Action Ind. Company 305 | Toano, VA, United States | Manufacturer, Repackager or relabeler | 1 | March 10, 2003 | 0 | 0 | 0 | api.fda.gov |
| B. Braun Medical Inc. | Bethlehem, PA, United States | Specification developer | 1 | September 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Baxter Healthcare Corporation | Round Lake, IL, United States | Complaint file establishment, Specification developer | 1 | May 14, 1996 | 0 | 0 | 0 | api.fda.gov |
| Baxter Productos Medicos, Ltda. | 1-7052 Cartago, Costa Rica | Manufacturer | 1 | May 14, 1996 | 0 | 0 | 0 | api.fda.gov |
| Baxter Healthcare, S.A. | Haina San Cristobal, Dominican Republic | Manufacturer | 1 | May 14, 1996 | 0 | 0 | 0 | api.fda.gov |
| Baxter Limited | Marsa, Malta | Specification developer | 1 | May 14, 1996 | 0 | 0 | 0 | api.fda.gov |
| Canadian Hospital Specialties Ltd. | OAKVILLE Ontario, Canada | Manufacturer | 1 | November 28, 2001 | 0 | 1 | 0 | api.fda.gov |
| DePuy Mitek, Inc. | Raynham, MA, United States | Specification developer | 1 | May 8, 1998 | 0 | 0 | 0 | api.fda.gov |
| Intl. Medsurg Connection, Inc. | Schaumburg, IL, United States | Specification developer | 1 | March 10, 2003 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | June 10, 1997 | 0 | 0 | 0 | api.fda.gov |
| Stryker Endoscopy | San Jose, CA, United States | Specification developer | 1 | October 25, 2004 | 0 | 1 | 0 | api.fda.gov |
| Stryker Puerto Rico, LLC. | Arroyo, PR, United States | Manufacturer | 1 | October 25, 2004 | 0 | 0 | 0 | api.fda.gov |
| Auris Health, Inc | Santa Clara, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Auris Health, Inc. | San Jose, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B. Braun Dominican Republic Inc. | SANTO DOMINGO Distrito Nacional, Dominican Republic | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B. Braun Us Device Manufacturing LLC | Allentown, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Changzhou DSB Medical Co., Ltd | Changzhou City Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gcmedica Enterprise Ltd. (wuxi) | Wuxi Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gebruder Renggli, AG | Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Honduras Kitting, S.A. | Villanueva Cortes, Honduras | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiangsu Shenli Medical Production Co.,ltd | CHANGZHOU Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | NEUHAUSEN OBECK Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nexus Medical, LLC | Lenexa, KS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Storz Endoskop Produktions GMBH | Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.