Conphar, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conphar, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CONPHAR SILICONE FEEDING TUBE, MAYO-HEGAR NEEDLE HOLDER, OLSEN HEGAR NEEDLE HOLDERS
122
Total
122
Cleared
0
Denied
Conphar, Inc. has 122 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 122 cleared submissions from 1979 to 1982.
Browse the FDA 510(k) cleared devices submitted by Conphar, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Conphar, Inc.
122 devices
Cleared
Aug 10, 1982
CONPHAR SILICONE FEEDING TUBE
Gastroenterology & Urology
49d
Cleared
Jun 03, 1982
MAYO-HEGAR NEEDLE HOLDER
General & Plastic Surgery
30d
Cleared
Jun 03, 1982
OLSEN HEGAR NEEDLE HOLDERS
General & Plastic Surgery
30d
Cleared
Jun 03, 1982
CONPHAR MAYO HEGAR NEEDLE HOLDER
General & Plastic Surgery
29d
Cleared
May 28, 1982
ROCHESTER PEAN FORCEPS
General & Plastic Surgery
25d
Cleared
May 28, 1982
MAYO SCISSOR STRAIGHT 6 3/4
Dental
25d
Cleared
May 28, 1982
MAYO SCISSOR STRAIGHT 5 1/2
Dental
25d
Cleared
May 28, 1982
MAYO SCISSOR CURYED 5 1/2
Dental
25d
Cleared
May 28, 1982
THUMB DRESSING FORCEPS 5
Dental
25d
Cleared
May 28, 1982
ADSON FORCEPS 4 3/4
Dental
24d
Cleared
May 28, 1982
SPLINTER FORCEPS 4 1/2
Dental
24d
Cleared
May 28, 1982
IRIS SCISSORS STRAIGHT 4 1/2
Ophthalmic
24d
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