# Onyx Medical Corp.

- Location (FDA's records): Memphis, TN
- FDA decisions: 48 (1990–2004): 48 510(k) clearances
- Names in FDA's records: Onyx Medical Corp. (47); Onyx Medical, Inc. (1)
- Product codes: HRS (14), HWC (11), JDR (3), KTT (3), LXH (3), JDI (2), JDW (2), KWL (2), HTY (2), ILY (1), KTW (1), KWK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 8 (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
- Ferguson Medical: 2 (https://510kreport.com/company/ferguson-medical)
- Compagnie Financiere & Medicale (Cf&M): 1 (https://510kreport.com/company/compagnie-financiere-medicale-cf-m)
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)
- Biopro, Inc.: 1 (https://510kreport.com/company/biopro)
- Ortho Solutions Limited: 1 (https://510kreport.com/company/ortho-solutions)
- Acumed, LLC: 1 (https://510kreport.com/company/acumed)
- Millennium Medical Technologies, Inc.: 1 (https://510kreport.com/company/millennium-medical-technologies)

## Its most-cited devices
- K903258: Hagie Pin (1990), cited by 3
- K903261: Rush Pin (1990), cited by 2
- K931687: Multiple Fragment Plate (1994), cited by 1
- K903252: Broad Self-Compressing Plate (1990), cited by 1
- K931681: Cannulated Navicular Screw (1994), cited by 1

## Recent decisions
- K041679: Cold Light; Cold Light MD; Gossamer Dermlight (Dec 16, 2004)
- K942022: Face-IT Shield (Jul 8, 1994)
- K931690: Spoon Plate (Jun 7, 1994)
- K931692: T-Plate (May 4, 1994)
- K931684: Epiphysis Plate (May 4, 1994)
- K934614: Mini Fragment Plate (May 4, 1994)
- K931680: Cannulated Cancellous Screw (May 4, 1994)
- K931683: Cloverleaf Plate (Apr 25, 1994)

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