Atlas FDA

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

EFA — Predicate Candidate Screening

25 FDA 510(k) clearances under this product code; the 50 most recent screened below.

70 daysmedian FDA review time
216 days90th percentile
25clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K192809Dental HandpieceMicro-Nx Co., Ltd.2020-08-253290
K163239SMARTmaticKaltenbach & Voigt GmbH2017-03-171190
K143465MASTERmatic LUXKaltenbach & Voigt GmbH2015-04-091260
K101172RDT3 HANDPIECE HEAD MODEL RDT3Redent Nova, Ltd.2010-07-27920
K093894ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLEAnthogyr2010-03-03750
K092446INTRA LUX HEAD 3 LDSYKaltenbach & Voigt GmbH & Co.2009-11-03850
K090055LOW & HIGH SPEED KITDpm USA Corp.2009-10-272920
K092412STRONG IMPLANT HANDPIECESSaeshin Precision Co., Ltd.2009-09-03280
K090676MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLESAnthogyr2009-05-22700
K070084MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROLEst. Anthogyr2007-03-08580
K061701HIGH SPEED AIR TURBINE HANDPIECES, PAR-4HEX/4HX SERIES (TWINJ. Morita USA, Inc.2006-08-25700
K061581EXCEL HIGH SPEED DENTAL HANDPIECEOrthosource, Inc.2006-08-16700
K040674IMPLANTOLOGY CONTRA ANGLES, ENDODONTIC CONTRA ANGLES, GENERAAnthogyr2004-06-301070
K013185TCM ENDO IIINOUVAG AG2001-11-28650
K002709RACE ENDODONTIC FILEAmc General, Inc.2000-11-17790
K973062TWIST RECIPROCATING DISPOSABLE PROPHY ANGLEMedidenta Intl., Inc.1997-10-09520
K971603STERILE SUREFLEX FILES AND INSTRUMENTSDentsply Intl.1997-06-04340
K971606STERILE FLEXOFILE FILES AND INSTRUMENTSDentsply Intl.1997-06-03330
K965238T1 CONTROL HIGH SPEED DENTAL HANDPIECESiemens AG1997-03-19780
K960260STAR TITAN SERIES MOTORS & ATTACHMENTSDentalez Group1996-03-28702
K960507STAR DENTAL PUSHBUTTON AUTOCHUCK REPLACEMENT TURBINE FOR MIDDentalez Group1996-03-28521
K960719STAR DENTAL 430 SERIES HIGH SPEED HANDPIECEDentalez Group1996-03-28361
K953865SPACELINE FEEL 21J. Morita USA, Inc.1996-03-202160
K873147USI DENTAL POLISHER. A/G-20Cranston Ind., Inc.1987-10-14640
K800163VIMEDIC SYSTEM TMMedical Systems Group of Viskay, Inc.1980-02-05110

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