Atlas FDA

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

Medicon Instruments, Inc. · Predicate Candidate Screening

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

183 daysmedian FDA review time
203 days90th percentile
6clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K936249MEDICON INSTRUMENTS UNIPOLAR COAGULATION ELECTRODESMedicon Instruments, Inc.1994-07-212030
K936246MEDICON INSTRUMENTS BIPOLAR FORCEPTS AND ELECTRODESMedicon Instruments, Inc.1994-07-212030
K936262DISSECTORS, FORCEPS, SCISSORS, DILATION SETS, AND GALL STONEMedicon Instruments, Inc.1994-07-011830
K936247MEDICON INSTRUMENTS TROCARS, TROCAR SLEEVES AND REDUCTION SLMedicon Instruments, Inc.1994-05-191400
K936248MEDICON INSTRUMENTS CHOLANGIOGRAPHY NEEDLES, GUIDE TUBES, INMedicon Instruments, Inc.1994-05-161370
K936250RETRACTORS, SPECULUM, CLIP APPLIER FOR TITANIUM CLIPS, 2-WAYMedicon Instruments, Inc.1994-05-121330

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