Atlas FDA

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

GEY — Predicate Candidate Screening

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

78 daysmedian FDA review time
160 days90th percentile
41clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.2005-05-17772
K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWERArthrocare Corp.2002-03-28300
K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)Depuyacromed2001-11-14900
K972308MEDNEXT 1000 DRILLMednext, Inc.1997-08-20610
K971941AQUA SPRAYBoyd Industries, Inc.1997-08-14790
K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., Inc.1997-07-29760
K971268BONE & MARROW CLLECTION SYSTEMBiomedical International Corp.1997-07-03870
K964252ORTHOCHUCKBuckman Co., Inc.1997-05-272150
K970530ANSPACH LUBRICATING SYSTEM IIThe Anspach Effort, Inc.1997-05-05821
K964073BME BONE DRILL BITSBiomedical Ent., Inc.1996-11-14340
K962789SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEMSmith & Nephew Endoscopy, Inc.1996-08-14280
K961901BONE & MARROW COLLECTION SYSTEMBiomedical Ent., Inc.1996-08-06820
K954470SURGIMOTORW.O.M. World of Medicine GmbH1995-12-08730
K951773PODOSPRAY DRILL SYSTEMDarco Intl., Inc.1995-10-261920
K952008KARL STORZ DRILLKARL STORZ Endoscopy-America, Inc.1995-07-26890
K9511183M MAXI-DRIVER II ELECTRIC SYSTEM3M Company1995-07-061180
K940535AUTO LUBE SYSTEMThe Anspach Effort, Inc.1994-03-21421
K934172ACRO-POLY, INC. HANDPIECE/ANGLEHEAD ACCESSORIES FOR SURGICALAcro-Poly, Inc.1993-10-27610
K932700CUTO(TM) TISSUE MORCELLATION SYSTEMLinvatec Corp.1993-10-151340
K925360ES-100 POWER SYSTEM, ES-100 SERIESElekta Instruments, Inc.1993-09-073200
K913262AESCULAP SURGICAL ACCESSORIESAesculap, Inc.1991-12-301600
K913369MICRO-AIRE MODEL 2060Micro Surgical Instruments Corp.1991-11-01950
K913266MICRO-AIRE MODEL 2050E/ELEC HANDPIECE/TROTTLELESSMicro Surgical Instruments Corp.1991-10-21900
K9053832710-000 OSCILLATING SAW, GENERAL ASSEMBLYMicro Surgical Instruments Corp.1991-06-182010
K904682VISTEK ELECTRONIC CONTROLLERVistek Corp.1990-12-18640
K900033MICRO-AIRE POWERED MICRO-SURGERY INSTRUMENTSMicro-Aire Surgical Instruments, Inc.1990-02-13420
K882654PHYSIOTRON(TM) MICROSURGICAL MOTOR & COOLING SYS.Surgical Innovators of America, Inc.1988-09-20830
K873475MICRO-TORQUE HAND ENGINE & ACCESS. DERMABRA. BURSMcghan Medical Corp.1987-09-11110
K873476MINI-MOTOR HAND ENGINE & ACCESS. DERMABRASION BURSMcghan Medical Corp.1987-09-11110
K853778THE DEXTRA PRECISION POWER UNITStorz Instrument Co.1985-11-13650
K853761DRILLING TEMPLATEOrthopedic Systems, Inc.1985-10-07280
K853762ISOMETRIC ACL DRILL GUIDEOrthopedic Systems, Inc.1985-10-07280
K850389MULTIPLE OUTLET MANIFOLDThe Anspach Effort, Inc.1985-03-18450
K843519MINUTEMAN CO2 MICROSURG LASER GEN SURGAmerican Surgical Laser, Inc.1984-12-07930
K843518MINUTEMAN C02 MICROSURG LASER PODIATRYAmerican Surgical Laser, Inc.1984-12-07930
K843517MINUTEMAN CO2 MICROSURG LASER DERMATOL-American Surgical Laser, Inc.1984-12-07930
K842475RICHARDS INTRA-ARTICULAR SHAVER MOTORRichards Medical Co., Inc.1984-09-17840
K841165ELECTRO SURGERY SYSTEMMicro-Aire Surgical Instruments, Inc.1984-06-05780
K830153RICHARDS INTRA-ARTICULAR SHAVER BLADESRichard'S Medical Equip., Inc.1983-02-28410
K812438SAGITTAL SAWBlack & Decker(Tm)1981-11-02680
K812437150 DRIVER REAMERBlack & Decker(Tm)1981-11-02680

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