Carrington Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carrington Laboratories, Inc. - FDA 510(k) Cleared Devices
15
Total
9
Cleared
0
Denied
Carrington Laboratories, Inc. has 9 FDA 510(k) cleared general & plastic surgery devices. Based in Dallas, US.
Historical record: 9 cleared submissions from 1989 to 2002.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carrington Laboratories, Inc.
15 devices
Cleared
Oct 17, 2002
CARRAKLENZ AND ULTRAKLENZ
General & Plastic Surgery
66d
Cleared
Oct 03, 2001
THE SALICEPT ORAL PATCH
General & Plastic Surgery
89d
Cleared
Dec 10, 1998
ALOE THERAPY ORAL RINSE
General & Plastic Surgery
90d
Cleared
Mar 03, 1997
RADIACARE ORAL WOUND RINSE
General & Plastic Surgery
90d
Cleared
Sep 12, 1996
CARRASYN HYDROGEL WOUND DRESSING,CARRAGAUZE PADS,CARRAGAUZE STRIPS,CARRASORB...
General & Plastic Surgery
94d
Cleared
Jul 11, 1996
CARASYN HYDROGEL WOUND PRODUCTS
General & Plastic Surgery
69d
Cleared
Mar 21, 1996
CARRASYN HYDROGEL WOUND DRESSING/FDG PADS/CARAGAUZE STRIPS/PADS (MODIFICATION)
General & Plastic Surgery
69d
Cleared
Oct 11, 1995
CASRRASYN ORAL WOUND DRESSING
General & Plastic Surgery
113d
Cleared
May 10, 1995
CARRASYN HYDROGEL WOUND DRESSING, FDG PADS, CARRAGAUZE PADS, STRIPS
General & Plastic Surgery
43d
Cleared
Nov 29, 1994
CARRASYN FDG
General & Plastic Surgery
78d
Cleared
May 04, 1994
CARRASYN ORAL WOUND DRESSING
General & Plastic Surgery
274d
Cleared
Jan 31, 1992
CARRINGTON WOUND DRESSING 4X4(TM)
General & Plastic Surgery
85d