# Whitmore Ent., Inc.

- Location (FDA's records): San Antonio, TX
- FDA decisions: 2 (1993–1993): 2 510(k) clearances
- Product codes: KPR (1), FWZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Ralph Lindel, D.C.: 1 (https://510kreport.com/company/ralph-lindel-dc)

## Its most-cited devices
- K933778: Whitmore Ankle X-Ray Extension (Axe) (1993), cited by 1

## Recent decisions
- K933778: Whitmore Ankle X-Ray Extension (Axe) (Dec 13, 1993)
- K931037: Whitmore Vacuum-Lock Spinal Frame (VLSF-100) (Jul 30, 1993)

Source page: https://510kreport.com/company/whitmore-ent