Johnson & Johnson International is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Johnson & Johnson International - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Johnson & Johnson International has 10 FDA 510(k) cleared medical devices. Based in New Brunswick, US.
Historical record: 10 cleared submissions from 1989 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Johnson & Johnson International Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Johnson & Johnson International
10 devices
Cleared
Jul 23, 1997
ULTIMA TPS CEMENTED STEM
Orthopedic
209d
Cleared
May 19, 1995
SYNTHETIC ABSORBABLE SUTURE
General & Plastic Surgery
225d
Cleared
Apr 11, 1995
TIELLE* HYDROPOLYMER DRESSING
General & Plastic Surgery
110d
Cleared
Aug 22, 1994
DERMIVIEW CLEAR TAPE
General & Plastic Surgery
95d
Cleared
Jul 06, 1993
BARRIER SAF-TE HYDROGEL DRAPE
General Hospital
383d
Cleared
Nov 09, 1992
P.F.C. MODULAR TOTAL KNEE SYSTEM, MODULAR PLUS
Orthopedic
103d
Cleared
Nov 21, 1990
BIOCLUSIVE(R) ABSORBENT DRESSING
General & Plastic Surgery
352d
Cleared
Aug 15, 1990
ORTHOSORB(R) ABSORBABLE PIN
Orthopedic
141d
Cleared
Apr 30, 1990
P.F.C. HIP SYSTEM NON-POROUS FEMORAL COMPONENT
Orthopedic
80d
Cleared
Sep 28, 1989
BIOCLUSIVE* TRANSPARENT FILM DRESSING - NEW CLAIM
General & Plastic Surgery
42d