# Freyja Healthcare, LLC

- Location (FDA's records): Boston, MA
- FDA decisions: 3 (2024–2026): 3 510(k) clearances
- Product codes: GCJ (2), HIF (1)
- 510(k) review time since 2016: median 128 days, against 122 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Buffalo Filter Co., Inc.: 1 (https://510kreport.com/company/buffalo-filter)

## Its most-cited devices
- K252640: VereSee Optical Veres Needle and Endoscopic Camera (2025), cited by 1
- K232464: VereSee Optical Veres Needle System (2024), cited by 1

## Recent decisions
- K261139: VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103) (Aug 13, 2026)
- K252640: VereSee Optical Veres Needle and Endoscopic Camera (Oct 20, 2025)
- K232464: VereSee Optical Veres Needle System (May 2, 2024)

Source page: https://510kreport.com/company/freyja-healthcare