# Pedicraft, Inc.

- Location (FDA's records): Jacksonville, FL
- FDA decisions: 5 (1982–1993): 5 510(k) clearances
- Product codes: FMS (3), FRP (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Cr Enterprises, LLC: 1 (https://510kreport.com/company/cr-enterprises)
- Plastic Surgery Solutions, LLC: 1 (https://510kreport.com/company/plastic-surgery-solutions)
- Alfred E Mann Inst. For Biomedical Engineering: 1 (https://510kreport.com/company/alfred-e-mann-inst-for-biomedical-engineering)

## Its most-cited devices
- K905629: Pedicraft Infant Reflux Wedge (1991), cited by 3

## Recent decisions
- K925817: Head & Foot End Drop Pedi-Crib (Apr 20, 1993)
- K925949: Pedicragt Bassinet (Apr 20, 1993)
- K905630: Infant Reflux Sling (Mar 13, 1991)
- K905629: Pedicraft Infant Reflux Wedge (Mar 13, 1991)
- K821773: Pedicraft Bed, Model B2944 (Jun 23, 1982)

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