Medical Instrument Development Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Instrument Development Laboratories, Inc. - FDA 510(k) Cleare...
22
Total
22
Cleared
0
Denied
Medical Instrument Development Laboratories, Inc. has 22 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1982 to 2011.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Instrument Development Laboratories, Inc.
22 devices
Cleared
Apr 08, 2011
ULTIMATE VIT ENHAMCER (UVE)
Ophthalmic
245d
Cleared
Apr 29, 2002
MID LABS AUTONOMOUS VIT ENHANCER (AVE)
Ophthalmic
40d
Cleared
Dec 10, 1999
VIT ENHANCER
Ophthalmic
101d
Cleared
Sep 19, 1997
DIGI-INJECTOR
Ophthalmic
179d
Cleared
Apr 10, 1995
UNIVIT PROBE
Ophthalmic
76d
Cleared
Jul 27, 1994
MICRODRIVE
Ophthalmic
306d
Cleared
Jun 03, 1994
SUPRA-VIT(TM)
Ophthalmic
366d
Cleared
Apr 01, 1994
MID LABS TWIN ILLUMINATOR
Ear, Nose, Throat
333d
Cleared
Jan 27, 1993
MID LABS, INC. VIT MATE
Ophthalmic
159d
Cleared
Jul 22, 1985
COMBINED MVS SYSTEMS
Ophthalmic
98d
Cleared
Apr 03, 1985
INFUSION SLEEVE - OPHTHALMIC
Ophthalmic
22d
Cleared
Mar 29, 1985
I/A HANDPIECE
Ophthalmic
28d