# Safepath Medical, Inc.

- Location (FDA's records): Amesbury, MA
- FDA decisions: 2 (2018–2024): 2 510(k) clearances
- Product codes: GAP (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (1 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
- Sm Eng Co., Ltd.: 3 (https://510kreport.com/company/sm-eng)
- Louisville Laboratories, Inc.: 1 (https://510kreport.com/company/louisville-laboratories)

## Its most-cited devices
- K180701: SafePath Suturing System (2018), cited by 1

## Recent decisions
- K222944: SafePath Sulturing System-Silk Suture, SafePath Sulturing System Polyamide Suture (Nylon) SafePath Sulturing System- Polypropylene Suture (Oct 18, 2024)
- K180701: SafePath Suturing System (Jun 25, 2018)

Source page: https://510kreport.com/company/safepath-medical