Medical Products Development, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Products Development, Inc. - FDA 510(k) Cleared Devices
13
Total
12
Cleared
0
Denied
Medical Products Development, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1980 to 1981. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medical Products Development, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Products Development, Inc.
13 devices
Cleared
Apr 23, 1981
MULTIMICRO SURGICAL CAUTERY
Ophthalmic
108d
Cleared
Apr 23, 1981
MULTIPERFECTEMP CAUTERY
Ophthalmic
108d
Cleared
Apr 23, 1981
REPLACABLE BATTERY PERFECTEMP CAUTERY
Ophthalmic
108d
Cleared
Feb 26, 1981
SURG-FLEX 10 LIGHT
General & Plastic Surgery
84d
Cleared
Feb 12, 1981
REPLACABLE BATTERY HI-TEMP CAUTERY
General & Plastic Surgery
38d
Cleared
Feb 12, 1981
MULTIHI-TEMP CAUTERY
General & Plastic Surgery
38d
Cleared
Feb 04, 1981
HITEMP. TM 2 LOOPTIP CAUTERY
General & Plastic Surgery
77d
Cleared
Jan 23, 1981
SURG-FLEX 5 SURGICAL LIGHT
General & Plastic Surgery
18d
Cleared
Jan 23, 1981
SURG-FLEX 15 SURGICAL LIGHT
General & Plastic Surgery
18d
Cleared
Jan 05, 1981
MICROSURG CAUTERY
Ophthalmic
Cleared
Nov 12, 1980
HI-TEMP LOOPTIP SURGICAL CAUTERY
General & Plastic Surgery
50d
Cleared
Jun 26, 1980
HI-TEMP SURGICAL CAUTERY
General & Plastic Surgery
20d