Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

KOA — Predicate Candidate Screening

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

43 daysmedian FDA review time
185 days90th percentile
44clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K182664FiXcisionAgency For Medical Innovations GmbH2018-12-07730
K950267URETHRAL SUTURE GUIDEApplied Medical Resources1995-01-3180
K932465LI VASECTOMYFemcare , Ltd.1994-03-022850
K921546VASOVASOSTOMY SETCook Urological, Inc.1993-07-024570
K931181VESITEC SUTURE PASSERVesitec Medical, Inc.1993-05-12640
K921304DDV LIGATORNorth American Medical, Inc.1992-10-052080
K922971NO-SCALPEL VASCETOMY INSTRUMENTSPilling Co.1992-09-23960
K921228BENDEREV PROTECT-A-PASS NEEDLEEimark Labs, Inc.1992-09-141850
K922192VAS DILATORCook Urological, Inc.1992-08-07880
K896058GRASPING FORCEPSAnnex Medical, Inc.1989-12-28710
K891352MARLOW ANAL SPECULUMSimpson/Basye, Inc.1989-06-231050
K890218MICROSURGICAL CYSTOTOMEKinetic Medical Products1989-01-2790
K864963STOMACH EVACULATOR - EWALD STYLEMedovations, Inc.1987-10-142960
K863273MARTIN MEDICAL PRO-SCOPE ANOSCOPEMartin Medical1986-11-04710
K852014EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINAEffner and Spreine Co.1985-08-07900
K852725BABCOCK TISSUE FORCEPS, 6-1/4 + SS 410 OR 420The Huxley Instrument Corp.1985-07-09130
K852726ALLIS TISSUE FORCEPS, 4X5 TEETH, 6+SS 410 OR 420The Huxley Instrument Corp.1985-07-09130
K851162AL ASKARI PERCUTANEOUS ACCESS NEEDLE HOLDERVan-Tec, Inc.1985-04-15240
K851112RANDALL KIDNEY STONE FORCEPS 817-144 PCS. QUARTERThe Huxley Instrument Corp.1985-04-03150
K851113RANDALL KIDNEY STONE FORCEPS 817-144 PCS. FULL CURThe Huxley Instrument Corp.1985-04-03150
K851111RANDALL KIDNEY STONE FORCEPS 817-84 PCS. HALF CURVThe Huxley Instrument Corp.1985-04-03150
K841387WESTON RECTAL SNAREImm Enterprises , Ltd.1984-05-09430
K834171OP-CON SURG. INSTRUMENT #3Imm Enterprises , Ltd.1984-04-041350
K834191JAKOBI SURGICAL INSTRUMENTS #3 17/18/19Imm Enterprises , Ltd.1984-03-221220
K834192JAKOBI SURG. INSTRUMENTS #3 21/22/24Imm Enterprises , Ltd.1984-03-221220
K841003PROBES, VARIOUSPremier Dental Products Co.1984-03-20110
K832677P-S MEDICAL BERLIN VISADUCT KITPudenz-Schulte Medical Research Corp.1983-12-081210
K830786DISIMETRIC RELEASE OF INSTRANETICS RADAmerican Convertors Div., American Pharmaseal1983-05-18680
K822401ST. MARK'S RECTAL BIOPSY FORCEPSKeymed, Inc.1982-08-27170
K820015URETHAL CUTTER CLAMPLone Star Medical Products, Inc.1982-02-22480
K813504ACESSORY TO MODIFIED FREEDING JEJUNOSTOMidwest Metabolic Support Group1982-01-07230
K811973FORDER RETRACTORSurgemed Marketing, Inc.1981-07-31210
K811693FORDER RETRACTORDacomed Corp.1981-06-26110
K811223VASOVASOSTOMY STABILIZER PLATFORM DEVBiomet, Inc.1981-05-21170
K810915THE SCOTT DIALMENZENSERTLone Star Medical Products, Inc.1981-05-08320
K810533CIRCLE NEPHROSTOMY TUBE INTRODUCERAmerican V. Mueller1981-03-11130
K802983THE INQUINAL RESORVOIR INSERTERLone Star Medical Products, Inc.1980-12-30390
K801273MAGILL CATHETER INTRO. FORCEPSJ. Sklar Mfg. Co., Inc.1980-07-28601
K800441RUDD-CLINIC HEMORRHOIDAL FORCEPSJ. Sklar Mfg. Co., Inc.1980-04-08400
K772134SYRINGE, IRRIGATION, PRE-FILLEDKendall Research Center1977-11-28140
K761229ANAL/RECTAL SYRINGEAce Orthopedic Manufacturing Co.1977-02-24760
K760715FLEXIBLE CUTTING SCISSORSV. Mueller O.V. Baxter Healthcare Corp.1976-10-21260
K760717FLEXIBLE BIOPSY FORCEPSV. Mueller O.V. Baxter Healthcare Corp.1976-10-21260
K760716FLEXIBLE FOREIGN BODY FORCEPSV. Mueller O.V. Baxter Healthcare Corp.1976-10-15200

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