Acrymed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acrymed, Inc. - FDA 510(k) Cleared Devices
14
Total
12
Cleared
0
Denied
Acrymed, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Lake Oswego, US.
Historical record: 12 cleared submissions from 1994 to 2009.
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 - Acrymed, Inc.
14 devices
Cleared
Oct 21, 2009
ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSING
General & Plastic Surgery
166d
Cleared
Feb 26, 2009
ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #B
General & Plastic Surgery
129d
Cleared
Sep 19, 2008
ACRYDERM ABSORBENT OXYGEN DRESSING
General & Plastic Surgery
24d
Cleared
Jul 10, 2007
ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GEL
General & Plastic Surgery
155d
Cleared
Oct 06, 2006
ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006
General & Plastic Surgery
157d
Cleared
Nov 08, 2001
ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101
General & Plastic Surgery
135d
Cleared
Sep 12, 2001
ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSING
General & Plastic Surgery
68d
Cleared
Oct 13, 2000
ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103
General & Plastic Surgery
25d
Cleared
Sep 21, 2000
MODIFICATION TO ACRYDERM SILVER ANTIMICROBIAL WOUND DRESSING, MODELS 1041,...
General & Plastic Surgery
31d
Cleared
Apr 17, 2000
ACRYDERM SILVER ANTI-MICROBIAL WOUND DRESSING, MODELS 1041, 1042, 1043, 1044,...
General & Plastic Surgery
326d
Cleared
Aug 19, 1999
ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033
General & Plastic Surgery
64d
Cleared
Mar 21, 1997
ACRYDERM GEL WOUND DRESSING
General & Plastic Surgery
24d