Ferris Mfg. Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ferris Mfg. Corp. - FDA 510(k) Cleared Devices
20
Total
12
Cleared
0
Denied
Ferris Mfg. Corp. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1978 to 2005.
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 - Ferris Mfg. Corp.
20 devices
Cleared
Feb 22, 2005
FERRIS POLYMEM STERILE BREAST PAD
General Hospital
636d
Cleared
Oct 22, 2003
FERRIS POLYMEM SILVER WOUND DRESSING
General & Plastic Surgery
181d
Cleared
Aug 25, 2000
FERRIS POLYMEM STERILE WOUND DRESSING WITH COLLAGEN
General & Plastic Surgery
42d
Cleared
Aug 27, 1999
FERRIS POLYOSTOMY STERILE WOUND DRESSING
General & Plastic Surgery
99d
Cleared
Apr 29, 1999
FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
General & Plastic Surgery
42d
Cleared
Mar 01, 1999
FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING
General & Plastic Surgery
70d
Cleared
Sep 22, 1998
POLYTUBE
General & Plastic Surgery
83d
Cleared
Jun 07, 1994
FERRIS POLYMEM HYDROPHILIC WOUND DRESSING
General & Plastic Surgery
356d
Cleared
May 18, 1990
FERRIS HYDROPHILIC DRESSING (ADD'L INDICATIONS)
General & Plastic Surgery
129d
Cleared
Mar 23, 1988
FERRIS HYDROPHILIC DRESSING
General & Plastic Surgery
56d
Cleared
Jan 14, 1988
DYNAFILM
General & Plastic Surgery
73d
Cleared
Dec 29, 1987
FERRIS ECG ELECTRODE W/HYDROGEL
Cardiovascular
106d