Tissue Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tissue Technologies, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Tissue Technologies, Inc. has 9 FDA 510(k) cleared medical devices. Based in Albuquerque, US.
Historical record: 9 cleared submissions from 1995 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tissue Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tissue Technologies, Inc.
9 devices
Cleared
Jul 24, 2000
SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR...
General & Plastic Surgery
17d
Cleared
May 19, 2000
SOFTFORM FACIAL IMPLANT
General & Plastic Surgery
65d
Cleared
Sep 22, 1998
SOFT TISSUE AUGMENTATION YUBE WITH INSERTION TOOL
General & Plastic Surgery
68d
Cleared
Nov 24, 1997
SOFTFORM FACIAL IMPLANT
General & Plastic Surgery
73d
Cleared
Jun 03, 1997
TRU-PULSE CO2 SURGICAL LASER
General & Plastic Surgery
91d
Cleared
Feb 12, 1997
TRU-PULSE LASER (MODIFIED)
General & Plastic Surgery
167d
Cleared
Sep 03, 1996
SOFT TISSUE AUGMENTATION TUBE (S.T.A.T.)
General & Plastic Surgery
69d
Cleared
Apr 01, 1996
SOFT TISSUE AUGMENTATION TUBE
General & Plastic Surgery
59d
Cleared
Jul 21, 1995
TRU-PULSE PULSED CO2 SURGICAL LASER SYSTEM
General & Plastic Surgery
81d