Derma Sciences, Inc. is one of 4896 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Derma Sciences, Inc. - FDA 510(k) Cleared Devices
22
Total
18
Cleared
0
Denied
Derma Sciences, Inc. has 18 FDA 510(k) cleared general & plastic surgery devices. Based in Old Forge, US.
Historical record: 18 cleared submissions from 1992 to 2015.
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 - Derma Sciences, Inc.
22 devices
Cleared
Nov 19, 2015
Medihoney Wound Gel
General & Plastic Surgery
219d
Cleared
Jun 25, 2015
MEDIHONEY WOUND DRESSINGS
General & Plastic Surgery
609d
Cleared
Jul 27, 2011
MEDIHONEY HYDROGEL SHEET DRESSINGS WITH ACTIVE LEPTOSPERMUM HONEY
General & Plastic Surgery
152d
Cleared
Feb 22, 2011
MEDIHONEY GEL DRESSING WITH ACTIVE MANUKA HONEY
General & Plastic Surgery
239d
Cleared
Jun 19, 2008
DERMA SCIENCES OTC MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY
General & Plastic Surgery
14d
Cleared
Apr 23, 2008
DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY
General & Plastic Surgery
77d
Cleared
Nov 07, 2007
MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEY
General & Plastic Surgery
19d
Cleared
Aug 12, 1997
DERMAGRAN WOUND MANAGEMENT SYSTEM
General & Plastic Surgery
172d
Cleared
Nov 27, 1996
DERMAGRAN HYDROPHILIC OINTMENT
General & Plastic Surgery
79d
Cleared
Nov 02, 1995
DERMAGRAN HYDROPHILIC WOUND DRESSING
General & Plastic Surgery
17d
Cleared
Nov 02, 1995
DERMAGRAN HYDROPHILIC OINTMENT
General & Plastic Surgery
17d
Cleared
Nov 02, 1995
DERMAGRAN WOUND DRESSING
General & Plastic Surgery
17d