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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Micro-Medical Devices, Inc. — Predicate Candidate Screening

8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

133 daysmedian FDA review time
168 days90th percentile
8clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K003695MICROSCOPE-STAINLESS STEEL/FIBER OPTIC: .5-2.6MM MODEL MMD 4Micro-Medical Devices, Inc.2001-02-14760
K983882MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSMicro-Medical Devices, Inc.1999-03-151330
K963675THE FLAT PANEL STEIRLE DRAPE SYSTEM(TM), VIDEO MONITOR STERIMicro-Medical Devices, Inc.1997-01-271360
K951482ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)Micro-Medical Devices, Inc.1995-09-141680
K951894ACCESS EXPANSION SYSTEMMicro-Medical Devices, Inc.1995-06-15520
K945656THE COUPLER/DRAPE(TM), VIDEO CAMERA STERILE DRAPEMicro-Medical Devices, Inc.1995-03-281310
K940141LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATHMicro-Medical Devices, Inc.1994-05-191280
K936213ARTHROSCOPES AND ACCESSORIESMicro-Medical Devices, Inc.1994-05-181400

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda