# Specs USA, Inc.

- Location (FDA's records): Sarasota, FL
- FDA decisions: 2 (1996–2000): 2 510(k) clearances
- Product codes: LPH (1), IYO (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (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
- Multigon Industries, Inc.: 1 (https://510kreport.com/company/multigon-industries)

## Firms that cite its devices most
- Eska Implants GmbH & Co.: 1 (https://510kreport.com/company/eska-implants)
- Urometrics, Inc.: 1 (https://510kreport.com/company/urometrics)

## Its most-cited devices
- K993027: Eska Modular Hip System (2000), cited by 1
- K946349: Stenodoc (1996), cited by 1

## Recent decisions
- K993027: Eska Modular Hip System (Apr 6, 2000)
- K946349: Stenodoc (May 24, 1996)

Source page: https://510kreport.com/company/specs-usa