FDA applicant

Tissue Technologies, Inc.

San Francisco, CA9 decisions1995–20000 recalls

FDA records 9 decisions for Tissue Technologies, Inc. (San Francisco, CA) from 1995 to 2000: 9 510(k) clearances. Most are in product codes FTL (Mesh, Surgical, Polymeric) and GEX (Powered Laser Surgical Instrument). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Tissue Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tissue Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tissue Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Tissue Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Tissue”

FDA records each applicant name separately; these may or may not be the same firm.

Tissue Culture Innovations 6 Tissue Science Laboratories, Plc 6 Tissue Regeneration Technologies, LLC 5 Tissue Technologies Holdings, LLC 2 Tissue Seal, LLC 1 Tissue Regenix Group Plc 1 Tissue Medical Lasers, Inc. 1 Tissue Regeneration Technologies, LLC Dba AS Softwave… 1 Tissue Culture Biologicals 1 Tissue Differentiation Intelligence, LLC 1 Tissue Culture Biotec, Inc. 1 Tissue Repair Company 1

Tissue Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Tissue”