Atlas FDA

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

Mettler Electronics Corp. — Predicate Candidate Screening

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

96 daysmedian FDA review time
208 days90th percentile
32clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K113017SYS*STIM 240Mettler Electronics Corp.2012-06-262590
K111482SONICATOR PLUS 920Mettler Electronics Corp.2011-08-25900
K091540MTD 4000Mettler Electronics Corp.2009-10-081351
K071137SONICATOR PLUS 940, MODEL ME940Mettler Electronics Corp.2007-08-01990
K053546SONICATOR 740, MODEL ME 740Mettler Electronics Corp.2006-05-041350
K043586LASER SYS*STIM 540, MODEL ME 540Mettler Electronics Corp.2005-05-061290
K042554AUTO THERM 390, MODEL ME 390Mettler Electronics Corp.2004-10-08180
K031017SYS*STIM 208 AND 208AMettler Electronics Corp.2003-05-30600
K023083SILBERG T.P.S., TISSUE PREPARATION SYSTEM, MODEL ME 800Mettler Electronics Corp.2003-02-281640
K022458AUTO*THERM 395, MODEL ME 395Mettler Electronics Corp.2002-09-26620
K013192SONICATOR PLUS 930, MODEL ME 930Mettler Electronics Corp.2001-10-17220
K984142SONICATOR PLUS 992, MODEL NUMBER ME 992 AND SONICATOR PLUS 9Mettler Electronics Corp.1999-02-09830
K984114SYS STIM 294, MODEL ME 294Mettler Electronics Corp.1999-02-09840
K964028SYS STIM 226Mettler Electronics Corp.1997-02-031190
K951916CC RIDER, MODEL ME180Mettler Electronics Corp.1995-10-041630
K943469SONICATOR 730Mettler Electronics Corp.1994-08-29410
K934846SONICATOR 716Mettler Electronics Corp.1994-03-231660
K934845SONICATOR 715Mettler Electronics Corp.1994-01-211050
K921436SONICATOR PLUSMettler Electronics Corp.1993-04-273980
K893879SYS*STIM 207AMettler Electronics Corp.1989-12-192070
K893878SYS*STIM 206AMettler Electronics Corp.1989-12-192070
K883080SYS*STIM 220Mettler Electronics Corp.1989-04-272800
K883228SONICATOR 720 (MODEL ME720)Mettler Electronics Corp.1988-08-18170
K880901SONICATOR 710 (MODEL ME710)Mettler Electronics Corp.1988-03-17150
K880602MODIFIED SONICATOR 720, MODEL ME720Mettler Electronics Corp.1988-02-25140
K873812SONICATOR 720 (MODEL ME720)Mettler Electronics Corp.1987-12-10830
K855249MIDIFICATION SYS*STIM 207 (MODEL-ME207)Mettler Electronics Corp.1986-03-28920
K860107SYS*STIM 206 (MODEL-ME 206)Mettler Electronics Corp.1986-03-28740
K853750SYS*STIM 207 MODEL ME 207Mettler Electronics Corp.1985-11-26780
K851735SYS STIM 206 MODEL ME206Mettler Electronics Corp.1985-11-192080
K851397SONICATOR 705 MODEL ME 705Mettler Electronics Corp.1985-07-02840
K850013SYS STIM 206(MODEL-ME 206) MUSCLE STIMULATORMettler Electronics Corp.1985-04-08960

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