# Synemed, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 9 (1981–1995): 8 510(k) clearances and 1 original PMA approval
- Product codes: HPT (3), LOI (1), HQF (1), BTA (1), HIH (1), HHI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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
- Womancare Global: 1 (https://510kreport.com/company/womancare-global)
- Acmi Corporation: 1 (https://510kreport.com/company/acmi)

## Its most-cited devices
- K813282: Synevac Vacuum Curettage Systems (1981), cited by 2

## Recent decisions
- K954037: Field Trend (Nov 17, 1995)
- P830080: Picolas Neodymiun-Yag Ophthalmic Laseer (Feb 17, 1987)
- K852936: The Fieldmaster Model 275 (Oct 15, 1985)
- K833274: Dermatology Handpiece-Ophth Laser (Dec 3, 1983)
- K831085: Synevac Vacuum Source Unit (Jun 8, 1983)
- K828585: Opthalas Photocoagulator (Jan 3, 1983)
- K822853: Model 200 Squid (Oct 18, 1982)
- K813282: Synevac Vacuum Curettage Systems (Dec 14, 1981)

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