# Endoprime, Inc.

- Location (FDA's records): Blue Ash, OH
- FDA decisions: 1 (2015–2015): 1 510(k) clearance
- Product codes: LFL (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
- Ethicon Endo-Surgery, Inc.: 4 (https://510kreport.com/company/ethicon-endo-surgery)

## Recent decisions
- K150271: Prime Adaptive Ultrasonic Scalpel System (May 29, 2015)

Source page: https://510kreport.com/company/endoprime