Atlas FDA

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

HGI · Predicate Candidate Screening

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

239 daysmedian FDA review time
581 days90th percentile
53clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K202915IRIS Thermocoagulator and Digital ColposcopeLiger Medical, LLC2021-04-232060
K152843Liger Medical HTU-110Liger Medical, LLC2016-06-242690
K130606FMWAND FERROMAGNETIC SURGICAL SYSTEMDomain Surgical, Inc.2014-01-033020
K121881DOMAIN SURGICAL SYSTEMDomain Surgical, Inc.2012-10-181140
K070877ENDOCERVICAL ELECTRODE # 2Modern Medical Equipment Mfg., Ltd.2007-07-271200
K061651FISCHER CONE BIOPSY EXCISOR, MODELS 900-150, 151, 152, 154, Apple Medical Corp.2006-10-201291
K022593THOMAS MEDICAL ELECTRODESThomas Medical, Inc.2002-11-01880
K003608SOVEREIGN BIPOLAR INSTRUMENTS FOR GYNECOLOGYAesculap, Inc.2001-02-20900
K002042TRUCONE ROTATIONAL CONE BIOPSY INSTRUMENT, MODEL 231812 - 23New England Medical Corp.2001-02-012110
K993527LOOP ELECTRODE, BALL ELECTRODEPalm Medical USA, Inc.2000-07-062620
K993777DISPOSABLE AND REUSABLE BALL AND LOOP ELECTRODESR-Group Intl.2000-05-251990
K983840WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED)Wallach Surgical Devices, Inc.1999-05-202020
K982739GYNEX ELECTRODESGynex Corp.1999-03-122180
K974138ROCKET ELECTRODEA & A Medical, Inc.1998-01-30880
K971986VALLEY FORGE BIPOLAR LOOPValley Forge Scientific Corp.1997-08-26890
K965245TBDUtah Medical Products, Inc.1997-07-031840
K963653WALLACH QUANTUM 2000 ELECTROSURGICAL SYSTEMWallach Surgical Devices, Inc.1997-06-112720
K963348WALLACH INTEGRATION UNITWallach Surgical Devices, Inc.1997-03-192050
K963852KSEA THERMOCOAGULATOR (MODEL 265100 20)KARL STORZ Endoscopy-America, Inc.1996-12-10760
K955756KARL STORZ POINT COAGULATOR, SEMM CROCODILE FORCEPS, MYOMA EKARL STORZ Endoscopy-America, Inc.1996-11-263430
K961460LWEET CONE BIOPSY INSTRUMENTApple Medical Corp.1996-11-192178
K952030LOOP/SQUARE ELECTRODEE & M Engineering, Inc.1996-07-314570
K955093ASPIRATION/COAGULATION ELECTRODE ACE-311 & ACE-511Utah Medical Products, Inc.1996-04-291740
K952483LEEP SYSTEM 1000CooperSurgical, Inc.1995-10-061290
K944450SURGI-LINK LLETZ NEEDLE ELECTRODE, LOOP ELECTRODE, SQUARE LOUnimed Surgical Products, Inc.1995-07-253160
K921791WALLACH LEAP 100 ELECTRO SURGERY SYSTEMWallach Surgical Devices, Inc.1995-05-0411150
K942986ELECTRODES (BLADE, BALL, NEEDLE, AND LOOP)Aaron Medical Industries1995-03-212930
K940191ELECTROSURGICAL LOOP ELECTRODENational Wire & Stamping, Inc.1994-12-303510
K941251FINESSE IEC/601Utah Medical Products, Inc.1994-12-122720
K925333SINGLE USE TUNGSTEN WIRE LEE LOOP ELECTRODEAspen Labs1994-09-277060
K925560ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODESZinnanti Surgical Instruments, Inc.1994-08-306650
K935634WALLACH LEEP PROCEDURE KITWallach Surgical Devices, Inc.1994-07-202390
K925478ELECTROSURGICAL ELECTRODEMegadyne Medical Products, Inc.1994-06-276060
K931541MODEL 26-0375, ELECTROSURGICAL GENERATORCameron-Miller, Inc.1994-06-014290
K931437MODEL 80-1983, ELECTROSURGICAL GENERATORCameron-Miller, Inc.1994-05-274310
K930132LEEP AND LLETZ ELECTRODESNordex Medical Corp.1994-05-044770
K926179SEDLACEK HANDLESimpson/Basye, Inc.1994-03-254720
K923570CRYOMEDICS LLETZ LOOPSCabot Medical Corp.1994-02-285910
K923628CERVICAL LOOP ELECTRODE & ROLLERBALL ELECTRODEBruce Mclucas1994-02-225810
K93133816 ELECTRODES (BLADE, BALL, NEEDLE & LOOP)Aaron Medical Industries1994-02-163370
K921386SUOP ELECTRODES FOR EXCISIONAL PROCEDURESSilver Creek Surgical1993-10-085640
K922206SURGISTATValleylab, Inc.1993-09-074830
K921884FORCE 2Valleylab, Inc.1992-12-152380
K921222FORCE 1CValleylab, Inc.1992-09-231940
K914367ELECTROSURGICAL GENERATOR MODEL ESU100/250/550Gyne-Tech Instrument Corp.1992-04-282100
K914329SURGITRON UNITS- ELECTRO SURG SYST GYN INDICATIONEllman Intl. Mfg., Inc.1992-04-021880
K912046SINGLE USE LEE ELECTRODEAspen Labs1992-03-053020
K913213SINGLE USE LEE ELECTRODEAspen Laboratories, Inc.1992-02-132090
K905263UTAH ESSUUtah Medical Products, Inc.1991-09-182990
K905747LEEP SYSTEM 6000 ELECTROSURGICAL UNIT AND ACCESSORCoopervision Surgical1991-09-172671

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