# Trice Medical, Inc.

- Location (FDA's records): King Of Prussia, PA
- FDA decisions: 4 (2014–2024): 4 510(k) clearances
- Names in FDA's records: Trice Medical, Inc. (3); Trice Medical (1)
- Product codes: HRX (3), LFL (1)
- 510(k) review time since 2016: median 33 days, against 89 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 5 (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
- Axis Surgical Technologies, Inc.: 1 (https://510kreport.com/company/axis-surgical-technologies)
- Tenex Health, Inc.: 1 (https://510kreport.com/company/tenex-health)

## Firms that cite its devices most
- Intravu, Inc.: 1 (https://510kreport.com/company/intravu)
- A.M. Surgical, Inc.: 1 (https://510kreport.com/company/am-surgical)
- E Surgical, LLC: 1 (https://510kreport.com/company/e-surgical)

## Its most-cited devices
- K162475: mi-eye 2, mi-eye 2 monitor (2016), cited by 4
- K141119: Camera Enabled Probe (2014), cited by 1

## Recent decisions
- K241700: Tenex 2nd Generation System (Nov 18, 2024)
- K212556: mi-eye 3 needlescope with cannula, mi-tablet 3 (Sep 15, 2021)
- K162475: mi-eye 2, mi-eye 2 monitor (Sep 16, 2016)
- K141119: Camera Enabled Probe (Jul 29, 2014)

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