# Kappler, Inc.

- Location (FDA's records): Guntersville, AL
- FDA decisions: 2 (1994–1994): 2 510(k) clearances
- Product codes: FXP (1), FYA (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
- Kappler USA: 1 (https://510kreport.com/company/kappler-usa)

## Its most-cited devices
- K932694: Kappler Pro/Vent Procedure Gown (1994), cited by 1

## Recent decisions
- K932738: Kappler Pro/Vent Boot (Mar 29, 1994)
- K932694: Kappler Pro/Vent Procedure Gown (Mar 29, 1994)

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