Atlas FDA

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

HJK — Predicate Candidate Screening

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

58 daysmedian FDA review time
159 days90th percentile
41clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K201909RxSight Contact LensRxsight, Inc.2020-09-10630
K173944Endocular Viewing Lenses and Silicone RingPhakos2018-10-253030
K151961Volk Disposable Iridotomy Lens, Volk Disposable Capsulotomy Volk Optical, Inc.2015-08-18330
K142715Sensor Medical Family of Vitrectomy Lenses and ProductsSensor Medical Technology, LLC2014-12-16850
K051630SUPER VIEW DISPOSABLE BIOM LENS SETInsight Instruments, Inc.2005-06-29120
K051103HAAG-STREIT CONTACT GLASSES STERY CUP, ACCESSORYHaag-Streit USA, Inc.2005-06-07390
K050623VOLK DISPOSABLE VITRECTOMY LENSES, MODELS VOLK FLAT SSV D, VVolk Optical, Inc.2005-03-28181
K033950DORC VITRECTOMY LENSES, MODEL 1284 SERIESDutch Ophthalmic Research Center (D.O.R.C.)2004-02-20600
K030054DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSESFci Ophthalmics, Inc.2003-02-26510
K023221CONTACT LASER & DIAGNOSTIC LENSESVolk Optical, Inc.2002-10-11141
K022413LUNEAU 3 MIRROR LENSLuneau SA2002-09-24620
K014170STAURENGHI WIDE FIELD SCANNING LASER LENSOcular Instruments, Inc.2002-03-04740
K012096DISPOSABLE VITRECTOMY LENSOcular Instruments, Inc.2001-08-24500
K971853ENDOVIEW SPPHIRE LENS SETAmerican Medical Devices, Inc.1997-08-06780
K933976MANDELKORN SUTURE LYSIS LENSOcular Instruments, Inc.1994-11-084520
K933264RITCH NYLON SUTURE LASER LENSOcular Instruments, Inc.1994-10-314820
K940107VIRECTOMY LENSVisionary Technologies of Miami, Inc.1994-09-062390
K943125QUADRASPHERIC FUNDUS LENSVolk Optical, Inc.1994-09-02650
K94142050 DEGREE HRI PRISM LENSOcular Instruments, Inc.1994-08-291590
K914051PEDIATRIC VITRECTOMY LENS SETOcular Instruments, Inc.1991-12-09900
K914117LANDERS HIGH REFRACTIVE INDEX VITRECTOMY LENS SETOcular Instruments, Inc.1991-11-13610
K912366MAINSTER HIGH MAGNIFICATION LASER LENSOcular Instruments, Inc.1991-06-25270
K910231NMR-K FUNDUS LASER LENSOcular Instruments, Inc.1991-01-28100
K896198MAINSTER WIDE FIELD LASER LENSOcular Instruments, Inc.1989-12-18520
K894421WOLDOFF PRISMATIC BICONCAVE LENSOcular Instruments, Inc.1989-10-04790
K875330HOSKINS-BARKAN GONIOTOMY LENS 10MMOcular Instruments, Inc.1988-02-26580
K875331BICONCAVE VITRECTOMY LENSOcular Instruments, Inc.1988-02-26580
K875087PEYMAN G. 12.12 YAG LASER LENSOcular Instruments, Inc.1988-02-19720
K875114HOSKINS-BARKAN GONIOTOMY LENS 9MMOcular Instruments, Inc.1988-02-19670
K87285518MM PEYMAN WIDE FIELD YAG LASER LENSOcular Instruments, Inc.1987-09-04490
K87213612.5MM PEYMAN WIDE FIELD YAG LASER LENSOcular Instruments, Inc.1987-06-19160
K87145025MM PEYMAN WIDE FIELD YAG LASER LENSOcular Instruments, Inc.1987-06-03510
K864304YANNUZZI FUNDUS LASER LENSOcular Instruments, Inc.1986-12-15450
K863911MAINSTER RETINA LASER LENSOcular Instruments, Inc.1986-12-12650
K864418LANDERS INDIRECT VITRECTOMY LENSOcular Instruments, Inc.1986-11-28180
K862868ABRAHAM YAG LASER LENSOcular Instruments, Inc.1986-08-21230
K862728HOSKINS NYLON SUTURE LASER LENSOcular Instruments, Inc.1986-08-21340
K863027SCHIRMER PERIPHERAL IRIDECTOMY LASER LENSOcular Instruments, Inc.1986-08-21100
K861648WISE IRIDOTOMY-SPINCTEROTOMY LENSOcular Instruments, Inc.1986-06-19500
K862094LENS-EZEInsight International, Inc.1986-06-19170
K781960SURGICAL EYE SHIELDConcept, Inc.1979-02-09800

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