Tecnol New Jersey Wound Care, Inc. - FDA 510(k) Cleared Devices
35
Total
34
Cleared
0
Denied
Tecnol New Jersey Wound Care, Inc. has 34 FDA 510(k) cleared medical devices. Based in Hammonton, US.
Historical record: 34 cleared submissions from 1976 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tecnol New Jersey Wound Care, Inc. Filter by specialty or product code using the sidebar.
35 devices
Cleared
Aug 23, 1991
MODIFICATION TECNOL FLUIDSHIELD SURGICAL MASKS
General Hospital
64d
Cleared
Jul 12, 1991
FLUIDSHIELD(TM) CONE CLASSIC(TM) II SURGICAL MASK
General Hospital
74d
Cleared
Jul 08, 1991
FLUIDSHIELD CONE CLASSIC II SURG MASK W/SPLASH VIS
General Hospital
69d
Cleared
Feb 27, 1990
TECNOL LAZER(TM) SURGICAL MASK
General Hospital
125d
Cleared
Jul 25, 1989
TECNOL SILK STRIP
General & Plastic Surgery
36d
Cleared
Jun 23, 1989
TECNOL GAITERS PRODUCT NUMBER 47725-010
General Hospital
36d
Cleared
May 30, 1989
TECNOL NASO-GASTRIC TUBE HOLDER
Gastroenterology & Urology
85d
Cleared
May 23, 1989
TECNOL SECURE-ALL TUBE HOLDER
Gastroenterology & Urology
78d
Cleared
Jan 17, 1989
TECNOL VARIABLE TENSION BANDAGE
General & Plastic Surgery
88d
Cleared
Jul 27, 1988
TECNOL SECURE-ALL PELVIC TRACTION BELT
Orthopedic
30d
Cleared
Jul 12, 1988
TECNOL CATHETER LEG STRAP
Gastroenterology & Urology
15d
Cleared
Jun 15, 1988
TECNOL TIGER PAWS PRODUCT NUMBER 47705-010
General Hospital
26d