# Perimetrics, Inc.

- Location (FDA's records): Newport Beach, CA
- FDA decisions: 3 (2008–2025): 3 510(k) clearances
- Product codes: EKX (3)
- Predicates its devices cite: 2 (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

## Its most-cited devices
- K232657: InnerView LC (2023), cited by 1
- K072213: Perimetrics Periometer (2008), cited by 1

## Recent decisions
- K251597: InnerView System (Sep 18, 2025)
- K232657: InnerView LC (Sep 1, 2023)
- K072213: Perimetrics Periometer (Aug 29, 2008)

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