# Dimeda Instrumente GmbH

- Location (FDA's records): Tuttlingen, DE
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: HDA (1)
- Predicates its devices cite: 2 (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
- Tekno Medical Optik-Chirurgie GmbH & Co.: 1 (https://510kreport.com/company/tekno-medical-optik-chirurgie)
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)

## Recent decisions
- K092827: Dimela Obsterical Forceps, Model 72.1 XX XX (Jan 8, 2010)

Source page: https://510kreport.com/company/dimeda-instrumente