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Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

Midmark Corp. — Predicate Candidate Screening

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

76 daysmedian FDA review time
181 days90th percentile
31clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K122643VANTAGE MODEL V5000, V5100, V5000C, V5100CMidmark Corp.2013-01-071311
K112380CLEARVISIONMidmark Corp.2011-11-22970
K090670MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZERMidmark Corp.2009-07-071160
K023348MIDMARK M9 ULTRACLAVE STEAM STERILIZERMidmark Corp.2003-03-031470
K003090MIDMARK PROCENTER INSTRUMENT DELIVERY SYSTEMMidmark Corp.2000-10-18150
K992744MIDMARK M4*9 EASYCLAVE STEAM STERILIZERMidmark Corp.2000-01-101470
K990189MODIFICATION OF: MIDMARK M-11 ULTRACLAVE STEAM STERILIZERMidmark Corp.1999-04-19890
K936181MIDMARK M-11 ULTRACLAVE STEAM STERILIZERMidmark Corp.1994-11-303381
K926463RITTERMODEL 75 EVOLUTION UNIV POW EXAM TABLE/ACCESMidmark Corp.1994-10-216660
K934744MIDMARK MAGNUM GENERAL SURGICAL TABLEMidmark Corp.1994-03-281750
K923730MODEL 561 C-ARM PROCEDURES STRETCHERMidmark Corp.1994-02-095620
K932719RITTER MODEL 158 AND 159 EXAM LIGHTSMidmark Corp.1993-12-021810
K930686MIDMARK SURGICAL LIGHTING SYSTEMSMidmark Corp.1993-07-301700
K915141712 PLASTIC SURGERY TABLE & ACCESORIESMidmark Corp.1992-01-09570
K911322MODEL #M9 ULTRACLAVE STEAM STERILIZERMidmark Corp.1991-08-261530
K910781#491 POWER OTOLARYNGOLY CH/#498 PROCED CTR & ACCESMidmark Corp.1991-05-15790
K904011MODEL #527 OPHTHALMIC STRETCHERMidmark Corp.1990-10-03350
K900432MODEL #M8 ELECTRONIC STERILIZERMidmark Corp.1990-07-271780
K894335MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STRMidmark Corp.1989-09-12600
K895016MODEL #510/515 GENERAL TRANSPORT STRETCHERMidmark Corp.1989-09-11340
K894134POWER EXAMINATION TABLE MODEL # 411Midmark Corp.1989-08-28760
K894144POWER EXAMINATION TABLE MODEL # 405Midmark Corp.1989-08-28760
K894017POWER PODIATRY CHAIR/TABLE #414, #416 & #417Midmark Corp.1989-07-14420
K852422MODEL 500 PEDIATRIC STRETCHER/CRIBMidmark Corp.1985-07-05280
K841505SURGI-MED TABLE MODEL 485-LTMidmark Corp.1984-04-25150
K831385LITHOTOMY CHAIR #415Midmark Corp.1983-06-02350
K822531MULTIPLE, ENT CABINET #448Midmark Corp.1982-09-28360
K822530MULTIPLE, ENT CHAIR #418Midmark Corp.1982-09-14220
K820823MULTIPLE, MODEL #17Midmark Corp.1982-04-21280
K811190THREE MODELS OF TABLES, STOOLS, & LIGHTSMidmark Corp.1981-05-0890
K810598X-RAY COLLIMATING DEVICESMidmark Corp.1981-04-10350

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