Atlas FDA

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

HTD — Predicate Candidate Screening

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

28 daysmedian FDA review time
90 days90th percentile
73clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K051281THE NEEDLE CATCHERE.D.Medical , Ltd.2005-09-081140
K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.1998-06-241970
K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.1998-06-241970
K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.1998-06-241970
K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical Technology1991-10-23480
K911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.1991-03-29110
K895212TIK EXTRAKTORInstruments of Sweden, Inc.1989-09-27400
K890373HEMORRHOIDAL FORCEPSKinetic Medical Products1989-02-03110
K890369GALL STONE FORCEPSKinetic Medical Products1989-02-03110
K890244TUBING CLAMP FORCEPSKinetic Medical Products1989-01-2790
K890258BONE CUTTING FORCEPS, SINGLE-ACTIONKinetic Medical Products1989-01-2790
K890262LUNG FORCEPSKinetic Medical Products1989-01-2790
K890238CATHETER FORCEPSKinetic Medical Products1989-01-2790
K890260BONE SHEARSKinetic Medical Products1989-01-2790
K890213MICROSURGICAL FORCEPSKinetic Medical Products1989-01-2790
K890246ARTERY FORCEPSKinetic Medical Products1989-01-2790
K890259RIB SHEARSKinetic Medical Products1989-01-2790
K890257BONE CUTTING FORCEPS, DOUBLE-ACTIONKinetic Medical Products1989-01-2790
K890263CILIA FORCEPSKinetic Medical Products1989-01-2790
K890234SUTURE CLIP REMOVERKinetic Medical Products1989-01-2790
K890226SURGICAL FORCEPSKinetic Medical Products1989-01-2790
K874950MICROSURGICAL INSTRUMENTSSolway, Inc.1987-12-30280
K874965MANUAL SURGICAL INSTRUMENTS FOR GENERAL USESolway, Inc.1987-12-30280
K874023LEVTECH CLAMP APPLIERLevtech, Inc.1987-11-06350
K873510SERRATED GRASPING FORCEPS, CURVED DOWNArthropedics, Inc.1987-11-02630
K873512SERRATED GRASPING FORCEPS, RIGHTArthropedics, Inc.1987-11-02630
K873504CUP BIOPSY FORCEPS, RIGHTArthropedics, Inc.1987-11-02630
K873506CUP BIOPSY FORCEPS, CURVED UPArthropedics, Inc.1987-11-02630
K873513SERRATED GRASPING FORCEPS, CURVED UPArthropedics, Inc.1987-11-02630
K873505CUP BIOPSY FORCEPS, CURVED DOWNArthropedics, Inc.1987-11-02630
K873503CUP BIOPSY FORCEPS, LEFTArthropedics, Inc.1987-11-02630
K873511SERRATED GRASPING FORCEPS, LEFTArthropedics, Inc.1987-11-02630
K871535SMILJANIC BONE REPOSITIONING FORCEPSLink America, Inc.1987-05-14240
K870881LOOSE BODY GRASPERSBowen & Company, Inc.1987-03-23180
K852720THUMB DRESSING FORCEPS, 5+SS 410 OR 420The Huxley Instrument Corp.1985-07-15190
K852715MAGILL FORCEPS, ADULT, 10 + SS 410 OR 420The Huxley Instrument Corp.1985-07-15190
K852727ROCHESTER - PEAN FORCEPS, STRAIGHT, 6-1/4+SSThe Huxley Instrument Corp.1985-07-15190
K852723FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420The Huxley Instrument Corp.1985-07-15190
K852722STERILIZING FORCEPS, 3-PRONGE, 11+SS 410 OR 420The Huxley Instrument Corp.1985-07-15190
K852728KELLY HEMOSTATIC FORCEPS, STRAIGHT 5-1/2+SSThe Huxley Instrument Corp.1985-07-15190
K852713RUSSIAN TISSUE FORCEPS, 6 + SS 410 OR 420The Huxley Instrument Corp.1985-07-15190
K852718ADSON TISSUE FORCEPS, 1X2 TEETH 4-3/4+SSThe Huxley Instrument Corp.1985-07-15190
K852729AALSTEAD MOSQ. FORCEPS, STRAIGHT, 5+SS 410 OR 420The Huxley Instrument Corp.1985-07-15190
K851770VARIOUS DRESSING TISSUE FROCEPS(GILLIES, JEANS, RAArtiberia1985-06-20560
K851769VARIOUS DRESSING/TISSUE FORCEPS(ENGLISH, THUMB, TRArtiberia1985-06-20560
K842819HOOK PUNCH FORCEPS FOR ARTHROSCOPYMedtech Industries, Inc.1984-08-14260
K834367SUTURE REMOVAL WOUND CLOSURE-INSTRU-Sterling Multi-Products, Inc.1984-05-301730
K840304CATEGORY 17-MICROBIOLOGY DEVICESImm Enterprises , Ltd.1984-05-01980
K840318CAT. 14-CLINICAL TOXIOLOGY DEVICESImm Enterprises , Ltd.1984-04-23900
K840766JANACEK TUBO-UTERINE IMPLANTATION SETCimed Intl., Inc.1984-04-23600

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