# Dolphin Medical Technologies, Inc.

- Location (FDA's records): Sarasota, FL
- FDA decisions: 2 (1998–1999): 2 510(k) clearances
- Product codes: HWC (2)
- Predicates its devices cite: 14 (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
- Ace Medical Co.: 2 (https://510kreport.com/company/ace-medical)
- Osteomed LP: 2 (https://510kreport.com/company/osteomed)
- Zimmer, Inc.: 2 (https://510kreport.com/company/zimmer)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Aesculap, Inc.: 2 (https://510kreport.com/company/aesculap)
- Howmedica Corp.: 2 (https://510kreport.com/company/howmedica)
- Alphatec Mfg., Inc.: 2 (https://510kreport.com/company/alphatec-mfg)

## Recent decisions
- K990019: DRG Medium Screw System (Mar 15, 1999)
- K973810: DRG Large Screw System (Jan 5, 1998)

Source page: https://510kreport.com/company/dolphin-medical-technologies