# Bethesda Medical Devices

- Location (FDA's records): Brunswick, OH
- FDA decisions: 2 (2025–2026): 2 510(k) clearances
- Names in FDA's records: Bethesda Medical Devices (1); Bethesda Medical Devices, LLC (1)
- Product codes: MAX (1), KWQ (1)
- Predicates its devices cite: 4 (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
- Infront Medical, LLC: 1 (https://510kreport.com/company/infront-medical)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Meditech Spine, LLC: 1 (https://510kreport.com/company/meditech-spine)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)

## Recent decisions
- K261309: Palisades™ Buttress Plate System (Jul 16, 2026)
- K252113: PRADO™ Lumbar Interbody Fusion System (Aug 5, 2025)

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