# Promedica Products, Inc.

- Location (FDA's records): Newport Beach, CA
- FDA decisions: 6 (1988–1992): 6 510(k) clearances
- Product codes: FXX (2), DWF (1), LZA (1), GAS (1), GAR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Peters Surgical: 1 (https://510kreport.com/company/peters-surgical)
- Resorba Medical GmbH: 1 (https://510kreport.com/company/resorba-medical)

## Its most-cited devices
- K913101: Peters Cardioflon (TM) Suture (1992), cited by 1
- K913102: Peters Cardionyl (TM) Suture (1992), cited by 1

## Recent decisions
- K913101: Peters Cardioflon (TM) Suture (Aug 12, 1992)
- K913102: Peters Cardionyl (TM) Suture (Aug 3, 1992)
- K892768: Patient Examination Gloves (Poly) (Jun 14, 1989)
- K883412: The Carpentier Trans-Mitral Ventricular Vent (TM) (Feb 8, 1989)
- K882883: C-Mask (Flat) (Aug 10, 1988)
- K882882: C-MASK (Aug 10, 1988)

Source page: https://510kreport.com/company/promedica-products