# Marina Medical Instruments, Inc.

- Location (FDA's records): Alpharetta, GA
- FDA decisions: 5 (2001–2005): 5 510(k) clearances
- Product codes: HHW (1), GDW (1), KGO (1), LKF (1), HHK (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (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
- Bioteque America, Inc.: 1 (https://510kreport.com/company/bioteque-america)
- Surgeon Surgical Instrumentation, Inc.: 1 (https://510kreport.com/company/surgeon-surgical-instrumentation)
- Humana USA, Inc.: 1 (https://510kreport.com/company/humana-usa)
- Bioteque Corp.: 1 (https://510kreport.com/company/bioteque)

## Firms that cite its devices most
- Crossbay Medical, Inc.: 1 (https://510kreport.com/company/crossbay-medical)

## Its most-cited devices
- K021876: Mas with or Without Syringe (2003), cited by 1

## Recent decisions
- K042534: Marina Medical Finger Protectors (May 10, 2005)
- K031463: Marina Medical Silicone Pessary (Nov 18, 2003)
- K021876: Mas with or Without Syringe (Apr 8, 2003)
- K023725: Hemorrhage Occluder Pin (Hop), Model 337-247 (Feb 3, 2003)
- K010296: Uterine Manipulator Injector Cannula, Model R57-450 (Apr 11, 2001)

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