# Tissue Technologies, Inc.

- Location (FDA's records): San Francisco, CA
- FDA decisions: 9 (1995–2000): 9 510(k) clearances
- Product codes: FTL (6), GEX (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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
- Tissue Science Laboratories, Plc: 3 (https://510kreport.com/company/tissue-science-laboratories)
- Argus Photonics Group: 1 (https://510kreport.com/company/argus-photonics-group)

## Its most-cited devices
- K973462: Softform Facial Implant (1997), cited by 1
- K002071: Softform Soft Tissue Augmentation Tube with Insertion Tool Modifications for Strands and Suture Holes (2000), cited by 1
- K952049: Tru-Pulse Pulsed CO2 Surgical Laser System (1995), cited by 1
- K000849: Softform Facial Implant (2000), cited by 1

## Recent decisions
- K002071: Softform Soft Tissue Augmentation Tube with Insertion Tool Modifications for Strands and Suture Holes (Jul 24, 2000)
- K000849: Softform Facial Implant (May 19, 2000)
- K982475: Soft Tissue Augmentation Yube with Insertion Tool (Sep 22, 1998)
- K973462: Softform Facial Implant (Nov 24, 1997)
- K970804: Tru-Pulse CO2 Surgical Laser (Jun 3, 1997)
- K963683: Tru-Pulse Laser (Modified) (Feb 12, 1997)
- K962496: Soft Tissue Augmentation Tube (S.T.a.T.) (Sep 3, 1996)
- K960481: Soft Tissue Augmentation  Tube (Apr 1, 1996)

Source page: https://510kreport.com/company/tissue-technologies