# Proact, Ltd.

- Location (FDA's records): State College, PA
- FDA decisions: 7 (1990–2006): 7 510(k) clearances
- Names in FDA's records: Proact, Ltd. (5); Proact, Inc. (1); Proact Co. (1)
- Product codes: FCG (3), LWE (1), JOW (1), KNW (1), IRP (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)
- Care Fusion: 1 (https://510kreport.com/company/care-fusion)
- Devon Medical, Inc.: 1 (https://510kreport.com/company/devon-medical)

## Its most-cited devices
- K003909: Proact 1 (2001), cited by 2
- K913306: Bone-Temno/Sternum-Temno (1991), cited by 1
- K926559: Proact Biopsy Needle Enchancements (1993), cited by 1

## Recent decisions
- K052243: Proact with Gel or Proact 1 (Apr 12, 2006)
- K003909: Proact 1 (Jun 13, 2001)
- K941256: Quick Core II (Jul 13, 1994)
- K926559: Proact Biopsy Needle Enchancements (Mar 22, 1993)
- K913306: Bone-Temno/Sternum-Temno (Nov 1, 1991)
- K902320: Bauer Flexi-Temno Biopsy Needle (Oct 1, 1990)
- K902319: Bauer Temno Biopsy Needle (Sep 6, 1990)

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