# Rema Medizintechnik GmbH.

- Location (FDA's records): Ft. Lauderdale, FL
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: HRX (1)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Smith & Nephew Dyonics, Inc.: 2 (https://510kreport.com/company/smith-nephew-dyonics)
- Linvatec Corp.: 2 (https://510kreport.com/company/linvatec)
- Arthronet Medical, Inc.: 1 (https://510kreport.com/company/arthronet-medical)
- Micro-Aire Surgical Instruments, Inc.: 1 (https://510kreport.com/company/micro-aire-surgical-instruments)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Future Medical Systems, Inc.: 1 (https://510kreport.com/company/future-medical-systems)
- Karl Storz Endoscopy: 1 (https://510kreport.com/company/karl-storz-endoscopy)

## Recent decisions
- K060172: Rema Shaver Blades (May 31, 2006)

Source page: https://510kreport.com/company/rema-medizintechnik