# Britt Corp., Inc.

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 17 (1979–2001): 17 510(k) clearances
- Product codes: GEX (3), JOW (3), EWG (2), HQF (2), LLF (1), DPS (1), HHR (1), IYO (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Compression Therapy Concepts, Inc.: 4 (https://510kreport.com/company/compression-therapy-concepts)
- Stortford Medical, LLC: 1 (https://510kreport.com/company/stortford-medical)
- Devon Medical, Inc.: 1 (https://510kreport.com/company/devon-medical)
- Suretek Medical: 1 (https://510kreport.com/company/suretek-medical)

## Its most-cited devices
- K991038: Vaso Press DVT System, Models VP500, VP501 (2000), cited by 4
- K003828: Vaso Press DVT Foot Garment #VP 520 (2001), cited by 3

## Recent decisions
- K003828: Vaso Press DVT Foot Garment #VP 520 (May 18, 2001)
- K991038: Vaso Press DVT System, Models VP500, VP501 (Jun 22, 2000)
- K974393: Vaso Press System (Mar 19, 1999)
- K860977: Model 545-45 for Neurological Surgical Application (Oct 16, 1986)
- K860975: Model 545-45 Laser for Ear, Nose & Throat (Jul 18, 1986)
- K860974: Model 545-45 Laser for Derma., Pod., Surgical (Jul 7, 1986)
- K860277: Model 525-25 Watt C02 Laser for Ear, Nose & Throat (May 6, 1986)
- K860273: Model 525 - 25 Watt CO2 Medical Laser/Podiatry (Apr 23, 1986)

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