Atlas FDA

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

GCT — Predicate Candidate Screening

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

78 daysmedian FDA review time
218 days90th percentile
47clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K093125ALPHAXENON LIGHT 180 W AND 300 WGimmi GmbH2010-01-271170
K082925XENON-100 SCB LIGHT SOURCE, MODEL 20132620KARL STORZ Endoscopy-America, Inc.2008-12-18780
K070376CONMED LINVATEC 300W XENON LIGHT SOURCEConmed Linvatec2007-08-201932
K040949VIADUCT MINISCOPE AND ACCESSORIESAcueity, Inc.2004-05-07250
K022490KSEA MEDI PACKKARL STORZ Endoscopy-America, Inc.2003-09-294270
K031994LINVATEC 300W XENON LIGHT SOURCELinvatec Corp.2003-08-21551
K023468ENDOSCOPIC LIGHT SOURCE XL180/L3World of Medicine Lemke GmbH2003-01-14900
K021717ENDOSCOPIC LIGHT SOURCE, MODEL XL300/L5World of Medicine Lemke GmbH2002-08-20890
K020889ENDOSCOPIC LIGHT SOURCE XL202/L3World of Medicine Lemke GmbH2002-06-05780
K013880DAYLITE XENON LIGHT SOURCESDesigns For Vision, Inc.2001-12-07140
K992050LUMENON XENON LIGHT SOURCEWalter Lorenz Surgical, Inc.1999-09-14890
K992540XENON LIGHT SOURCE PES 1Laser Optik Systeme GmbH & Co. KG1999-09-14470
K983628XENON LIGHT SOURCE AUTO LIP 5123, MODEL 2123.011Richard Wolf Medical Instruments Corp.1998-12-11570
K982962XENON LIGHT SOURCE, MODELS LS6180, LS6035Contec Medical Vision, Ltd.1998-09-23300
K981804XENON LIGHT SOURCE MODEL LS6000Contec Medical Vision, Ltd.1998-07-24640
K980281WELCH ALLYN XENON 300 LIGHT SOURCEWelch Allyn, Inc.1998-02-27320
K971057COGENLIGHT TECHNOLOGIES XLS ILLUMINATOR SYSTEMCogent Light Technologies, Inc.1997-03-2840
K963227WHITE SUN LIGHT SOURCE MODEL #: XL300 AND #: XL175Products For Medicine1996-10-23650
K963044ENDOBEAMCorin USA1996-09-20460
K962365XENON LIGHTSOURCEDsp Worldwide1996-07-18290
K954561XENON NOPPVAKARL STORZ Endoscopy-America, Inc.1995-10-19170
K953924XLS-300 XENON LIGHT SOURCESpecialties of Surgery1995-09-21340
K952028COLD LIGHT SOURCE LOS XL-A 100Laser-Optik-Systeme GmbH & Co. KG1995-07-27870
K952563THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEMThe Tulip Mfg. Co.1995-07-25530
K952696XENON LIGHT SOURCE MODEL 5121Richard Wolf Medical Instruments Corp.1995-07-25420
K951971XENON LIGHT SOURCEEnvision Medical Corp.1995-05-24270
K951895ACCU-BEAM 300W XENON LIGHT SOURCETti Medical1995-05-24300
K944607MODEL 5135 AUTO LP/FLASHRichard Wolf Medical Instruments Corp.1994-12-13850
K944821MODEL 5151Richard Wolf Medical Instruments Corp.1994-11-14460
K934559KARL STORZ XENON LIGHT SOURCE MODEL 201320-20KARL STORZ Endoscopy-America, Inc.1994-04-222180
K940270LCI-100 AND LCI-200 WELCH ALLYN ILLUMINATION AND IMAGING SYSWelch Allyn, Inc.1994-04-20890
K936198ZEISS SUPERLUX HIGH-INTENSITY LIGHT SOURCESCarl Zeiss, Inc.1994-04-06980
K933405COGENT LIGHT ILLUMINATOR 10010 XENON LIGHT SOURCECogent Light Technologies, Inc.1994-02-182210
K935423COOL LIGHT 300Endosurgical Development Corp.1994-01-26780
K933868ANGIOLAZ VIDEO ENDOSCOPIC SYSTEM MODEL CAMLUM1 AND ACCESSORIAngiolaz, Inc.1993-11-10960
K932281VERRES NEEDLESurgeon Surgical Instrumentation, Inc.1993-08-06860
K924897XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300Medical Devices, Inc.1993-07-062800
K921315PENTAX XENON LIGHT SOURCEPentax Precision Instrument Corp.1993-06-254640
K923210SYSTEM 3000 XENON VIDEOLAP LIGHTCabot Medical Corp.1992-10-05960
K921390XENON LIGHT SOURCE AND ACCESSORIESCoopervision Surgical1992-07-271260
K913586MARLOW VERRES NEEDLESMarlo Surgical Technology1991-10-08570
K912354OLYMOUS XLS XENON LIGHT SOURCEPerkinelmer Optoelectronics1991-08-16800
K911492ENDOSCOPIC LIGHT SOURCEUnited States Endoscopy Group, Inc.1991-08-141320
K905282ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCEFrantz Medical Development, Ltd.1991-03-191160
K905124MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCERed Wing Imaging, Inc.1991-01-25720
K864801THE KEYMED HI-LIGHT 250 LIGHT SOURCEKeymed, Inc.1986-12-24150
K792215PENTEX UPPER G.I. SCOPE MODEL FG-28APentax Precision Instrument Corp.1979-12-10350

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