# Denver Splint Co.

- Location (FDA's records): Englewood, CO
- FDA decisions: 4 (1993–1994): 4 510(k) clearances
- Product codes: EMX (1), GEI (1), KGX (1), LRD (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
- Shippert Medical Technologies Corp.: 1 (https://510kreport.com/company/shippert-medical-technologies)

## Its most-cited devices
- K935724: The Expandacell Sinus Pack (1994), cited by 1

## Recent decisions
- K940798: Shippert Pressure Bandage (Sep 28, 1994)
- K940133: The Expandacell Ear Pack (May 23, 1994)
- K935724: The Expandacell Sinus Pack (May 12, 1994)
- K922062: The Denver Cautery (Jan 12, 1993)

Source page: https://510kreport.com/company/denver-splint