# Whiteside Instruments

- Location (FDA's records): Creve Coeur, MO
- FDA decisions: 1 (1996–1996): 1 510(k) clearance
- Product codes: LPH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K955271: Micro-Seal Acetabular System (Jan 30, 1996)

Source page: https://510kreport.com/company/whiteside-instruments