Atlas FDA

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

KNF — Predicate Candidate Screening

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

130 daysmedian FDA review time
413 days90th percentile
44clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K250705Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2025-04-02230
K240503Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2024-07-171470
K233848Sonata Transcervical Fibroid Ablation System 2.2 (SONATA2-22Gynesonics, Inc.2023-12-21160
K222304Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2022-11-08990
K211535Sonata Transcervical Fibroid Ablation System 2.2Gynesonics, Inc.2021-06-17300
K193516Sonata® Sonography-Guided Transcervical Fibroid Ablation SysGynesonics, Inc.2020-05-041370
K173703Sonata Sonography-Guided Transcervical Fibroid Ablation SystGynesonics, Inc.2018-08-152540
K132135LINA GOLD LOOP HCLina Medical Aps2014-01-312050
K121343MODULAP LOOPAtc Technologies, Inc.2013-06-144060
K103726JARIT TAKE-APART ENDOSCOPIC INSTRUMENTSIntegra LifeSciences Corporation2012-02-084131
K092897LAP LOOPMedsys, S.A.2010-02-011330
K070315LINA LOOP, MODELS: EL-160-4, EL-160-8, EL-200-4, EL-200-8Lina Medical Aps2007-10-302713
K022979LAPARETTE, MODEL LAP J L S H NInstruments Medicaux G.B., Inc.2002-12-181000
K010752AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGYAesculap, Inc.2001-06-11900
K003405ENDOSCOPIC MONOPOLAR FORCEPS-SCISSORS, EMF-2000 TO 2999,ENDOHighland / Marietta, Inc.2001-05-071870
K010425EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)Hdc Corp.2001-03-15300
K981463OMNITECH RESECTOSCOPE ROLLER ELECTRODEOmnitech Systems, Inc.1998-07-17850
K981464OMNITECH RESECTOSCOPE CUTTING LOOP ELECTRODEOmnitech Systems, Inc.1998-07-10780
K970961VAPORIZATION ELECTRODESRichard Wolf Medical Instruments Corp.1998-04-103890
K972856ULTRA-FINE DIATHERMY LOOP AND COAGULATION BALLSRocket Medical Plc1998-02-111940
K971838MICRO ELECTRODESCooperSurgical, Inc.1997-11-051700
K971146LAPARETTERd Chus, Inc.1997-08-251500
K964594VAPORTRODE VAPORIZATION ELECTRODE -GROOVED/FLUTED/SPIKED(GVECircon Corp.1997-08-152730
K971621RESISTICK SOLID LAPAROSCOPIC ELECTRODESAaron Medical Industries1997-06-20500
K964441FEMRX FOCUSED MONOPOLAR (FAP) OPERASTAR SYSTEM [OUTPATIENT EGynecare Innovation Center1997-03-281420
K953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESSymbiosis Corp.1995-10-06870
K952070NEZHAT-DORSEY ELECTROSURGICAL HAND CONTROL ATTACHMENTS, PENCAmerican Hydro-Surgical Instruments, Inc.1995-07-26850
K950499NEZHAT-DORSEY LAPAROSCOPIC HAND INSTRUMENTSAmerican Hydro-Surgical Instruments, Inc.1995-06-161300
K944862KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION KARL STORZ Endoscopy-America, Inc.1995-02-091290
K944793KARL STORZ MONOPOLAR COAGULATION, NEEDLE, LOOP ELECTRODESKARL STORZ Endoscopy-America, Inc.1995-01-241180
K941207MONOPOLAR SUCTION CANNULA; MONOPOLAR ELECTRODESNew Eder Corp.1995-01-243160
K944300KARL STORZ INSULATED BIOPSY FORCEPSKARL STORZ Endoscopy-America, Inc.1994-12-151000
K944297KARL STORZ INSULATED SCISSORSKARL STORZ Endoscopy-America, Inc.1994-12-151000
K933300GEISTER SURGICAL INT'L MONOPOLAR ENDOSCOPIC SURG.INST.Lyle Howard Corp.1994-09-304500
K921727CORE MONITORING SYSTEM-SP1475/6275/5607/5708/4575Viggo-Spectramed1994-05-107600
K932456JARIT SURGICAL INSTRUMENTSJ. Jamner Surgical Instruments, Inc.1994-04-213351
K921686ENDOMED LAPAROSCOPY INSTRUMENTSBuckman Co., Inc.1994-03-307210
K935947HI-TOPS ELECTRODES 14-8000W. J. Medical Instruments, Inc.1994-02-28770
K924200REFLEX(R) ESCRichard-Allan Medical Ind., Inc.1994-02-225510
K902658GYNESCOPE MONOPOLAR FORCEPS AND ELECTRODESGynescope Corp.1990-09-19960
K871960ELECTRO-GYNE ELECTROSURGICAL GENERATORCabot Medical Corp.1987-07-10510
K780955SCISSORS, HOOK, ELECTROSURGICALKli1978-06-22130
K780954SCISSORS, HOOK, ELECTROSURGICALKli1978-06-22130
K772220PROBE, COAGULATION ACCESSORYKli1977-12-1380

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