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Medical Instrument Development Laboratories, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
23
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K153168Bi-Blade Vitrectomy CutterApril 29, 2016
K102222ULTIMATE VIT ENHAMCER (UVE)April 8, 2011
K020911MID LABS AUTONOMOUS VIT ENHANCER (AVE)April 29, 2002
K992943VIT ENHANCERDecember 10, 1999
K971067DIGI-INJECTORSeptember 19, 1997
K950287UNIVIT PROBEApril 10, 1995
K934600MICRODRIVEJuly 27, 1994
K932669SUPRA-VIT(TM)June 3, 1994
K932131MID LABS TWIN ILLUMINATORApril 1, 1994
K924222MID LABS, INC. VIT MATEJanuary 27, 1993
K851610COMBINED MVS SYSTEMSJuly 22, 1985
K851009INFUSION SLEEVE - OPHTHALMICApril 3, 1985
K850857I/A HANDPIECEMarch 29, 1985
K844761SCHWARTZ/NORRIS CORNEAL LIGHT SHIELDDecember 24, 1984
K842793MVS XIIDecember 19, 1984
K843391INFUSION ASPIRATION VITRECTOMY SYSDecember 19, 1984
K844131NUCLEOTOMENovember 29, 1984
K842471AUTOMATED INTRAOCULAR SCISSORSNovember 21, 1984
K834537MICRO VIT FRAGMENTATION SYSTEMMarch 16, 1984
K831584BAILEY ASPIRATOR/IRRIGATORAugust 12, 1983