# Coaptech, Inc.

- Location (FDA's records): Baltimore, MD
- FDA decisions: 3 (2019–2025): 3 510(k) clearances
- Names in FDA's records: Coaptech, Inc. (2); Coaptech, LLC (1)
- Product codes: KGC (3)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Kimberly-Clark Corp.: 1 (https://510kreport.com/company/kimberly-clark)

## Its most-cited devices
- K183057: PUMA-G System (2019), cited by 1
- K223916: PUMA-G System (2023), cited by 1

## Recent decisions
- K242211: PUMA-G Pediatric System (Apr 29, 2025)
- K223916: PUMA-G System (Mar 29, 2023)
- K183057: PUMA-G System (Apr 10, 2019)

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