# Rotec Medizintechnik GmbH

- Location (FDA's records): Weisendorf, DE
- FDA decisions: 2 (2000–2000): 2 510(k) clearances
- Product codes: LZO (2)
- Predicates its devices cite: 6 (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
- Biomet, Inc.: 3 (https://510kreport.com/company/biomet)
- Osteonics Corp.: 1 (https://510kreport.com/company/osteonics)
- Link America, Inc.: 1 (https://510kreport.com/company/link-america)
- Johnson & Johnson Professionals, Inc.: 1 (https://510kreport.com/company/johnson-johnson-professionals)

## Recent decisions
- K992359: MRS-Titan (Feb 18, 2000)
- K992403: MRP-Titan (Jan 21, 2000)

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