510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960481Substantially Equivalent

Soft Tissue Augmentation Tube

Tissue Technologies, Inc., San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960481 is the FDA 510(k) clearance record for SOFT TISSUE AUGMENTATION TUBE, a class II device, cleared for Tissue Technologies, Inc. on under FDA product code FTL (Mesh, Surgical, Polymeric). FDA records list 9 510(k) clearances for Tissue Technologies, Inc., from to . As of , FDA records show no recalls naming K960481.

Clearance record

Decision date
Received
(59 days to decision)
Product code
FTL Mesh, Surgical, Polymeric
Regulation
21 CFR 878.3300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Tissue Technologies, Inc. 1370 Green St., San Francisco CA
510(k) summary
Statement
Third party review
No

Clearances, product code FTL

Trailing 12 months
1 clearance under product code FTL in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260