# Teknomed, Inc.

- Location (FDA's records): Danvers, MA
- FDA decisions: 7 (1979–1993): 7 510(k) clearances
- Product codes: GEX (3), FFK (2), LNK (1), IZF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K925395: Technomed Pulsolith 4000 Laser System (May 21, 1993)
- K913917: Multilase 2100 C, 2100 D (Nov 5, 1992)
- K920708: Multilase 2500 a (Nov 5, 1992)
- K913290: Multilase 2100 a (Feb 21, 1992)
- K895178: Technomed Pulsolith Laser System (Oct 6, 1989)
- K890436: Technomed Pulsolith Laser System (Mar 23, 1989)
- K790132: Tecnotomo (Feb 21, 1979)

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