Atlas FDA

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

HKX — Predicate Candidate Screening

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

106 daysmedian FDA review time
330 days90th percentile
58clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K253039AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIATopcon Corporation2025-11-07460
K223739VS Tabletop TonometerMedimaging Integrated Solution, Inc.2023-11-083290
K190382Intraocular Pressure Tonometer EASYTONCompany Elamed2019-12-062900
K181260MiiS Horus Scope DPT 100Medimaging Integrated Solution, Inc (Miis)2019-06-214060
K181143Keeler TonoCare TonometerKeeler Instruments, Inc.2019-02-082830
K180820Tono Vue Non-Contact TonometerCrystalvue Medical Corporation2018-12-142600
K162067VX130 Ophthalmic Diagnostic DeviceLuneau Sas2017-04-242720
K143086VX120 Ophthalmic Diagnostic DeviceLuneau Sas2015-06-012170
K113066CORVIS STOculus Optikgerate GmbH2012-11-083880
K111710FULL AUTO TONOMETER MODEL TX-20Canon Inc. -Medical Equipment Group2011-09-20920
K093298PULSAIR INTELLIPUFF, PULSAIR DESKTOP MODEL 2414-P-2001, 2417Keeler Instruments, Inc.2010-12-104150
K083377ACCUPENAccutome Ultrasound, Inc.2009-07-272550
K073087NON-CONTACT TONOMETER, MODEL FT-1000Tomey Corporation2008-11-183830
K081756OCULAR RESPONSE ANALYZERReichert, Inc.2008-08-07480
K053444KOWA KT-800Kowa Co. , Ltd.2006-06-091820
K060780TONOMETER DIATONRyazan State Instruments2006-04-06150
K042099TONOPACH ULTRASONIC TONOMETER/PACHYMETER MODEL P-201 (THE TORetinapharma Technologies, Inc.2004-12-101280
K032799NON-CONTACT TONOMETERS, OCULAR RESPONSE ANALYZERReichert, Inc.2004-01-201330
K031733NON-CONTACT TONOMETER, MODEL NT-4000Nidek, Inc.2003-12-041830
K023676APPLANATION TONOMETEROptilasa, S.L.2003-04-241740
K023816CANON FULL AUTO TONOMETER TX-FCanon, Inc.-Utsunomiya Optical Products Operation2002-11-26110
K013805KOWA AUTOMATED TONOMETER KT-500Kowa Optimed, Inc.2002-10-113300
K021937TGDC-01 PRATruevision Instruments2002-10-111210
K013259PORTABLE NON-CONTACT TONOMETER, MODEL PT100Leica Microsystems, Inc. O.I.D.2002-02-201420
K010998LANGHAM OCULAR BLOOD FLOW (OBF) TONOGRAPH/TONOMETER MODEL 20Langham Ophthalmic Technologies2001-06-27850
K002395MODEL 30 CLASSIC PNEUMATONOMETERXomed, Inc.2000-12-111260
K002510SMARTLENSOdc Ophthalmic Development Co. AG2000-10-18640
K990869LEICA AT550Leica Microsystems, Inc.1999-06-07830
K990257KEELER PULSAIR 3000 NON CONTACT TONOMETERKeeler Instruments, Inc.1999-03-25570
K963079CANON TX-10 TONOMETERCanon USA, Inc.1997-03-032080
K953031ZEIMER SELF TONOMETERCds Technologies1995-08-22900
K945972DIGITAL AVERAGING TONOMETEROpti-Med Electronics1995-08-172520
K943939NON-CONTACT TONOMETER T-2Canon, Inc.1995-05-122730
K941865XPERT NCTReichert Ophthalmic Instruments, Div. Leica, Inc.1994-09-291640
K921443TIP & MEMBRANE ASSEMBLYBio-Rad1993-06-224830
K924777BURTON APPLANATION TONOMETER - MODEL T850 & T1000R.H. Burton Co.1993-04-051940
K921617CYLINDER OF GAS, CAN OF GAS (CC12F2)Bio-Rad1992-08-051210
K913189NIDEK MODEL NT-1000Nidek, Inc.1991-10-15890
K911721KEELER PULSAIR NON CONTACT TONOMETER, MODIFICATIONKeeler Instruments, Inc.1991-06-25690
K895575BIO-RAD MODULAR AIR COMPRESSORBio-Rad1989-10-31470
K884012MMAC II TONOMETERProfessional Technologies Corp.1989-01-061060
K873422OBF MODEL 115 COMPUTER TONOMETER SYSTEMOcular Blood Flow Laboratories, Inc.1987-11-02680
K873917TONOMETER TAPESRichmond Products, Inc.1987-11-02380
K871935T P C (TONOMETER PROBE COVER)Krb Ent.1987-06-03150
K871335TOPCON COMPUTERIZED TONOMETER CT-10Topcon Instrument Corporation of America1987-05-18450
K870750KEELER PULSAIR NON CONTACT TONOMETERKeeler Instruments, Inc.1987-03-17200
K870121DIGILAB MICRO ONE APPLANATION TONOMETERBio-Rad1987-02-20390
K864959OBF MODEL 112 VACUUM CUP SYSTEMOcular Blood Flow Laboratories, Inc.1987-02-12560
K863235SURGICAL IOP MONITORAmeritek, Inc.1986-09-25350
K863217DIGILAB MODULAR ONE-APPLANATION TONOMETERBio-Rad1986-09-24350

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