Atlas FDA

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

GDX — Predicate Candidate Screening

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

32 daysmedian FDA review time
113 days90th percentile
26clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K923689SURGISTAR BLADESSurgistar, Inc.1992-09-09470
K921167ULTRABLADEMicron Technology, Inc.1992-07-301410
K914086ICAN CYLINDRICAL SPONGESIcn Pharmaceuticals, Inc.1991-10-09280
K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.1991-04-232030
K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.1990-12-13130
K895682VESSEL LOOPSApplied Medical Technologies1989-10-24330
K893033MINI-DIAMOND KNIFEL.A.B. Instruments1989-05-26320
K880028OMED DISPOSABLE SCALPELOxboro Medical Intl., Inc.1988-01-29240
K871894KCK INDUSTRIES' SURGICAL INSTRUMENTSKck Industries1987-06-23530
K863950P.S.I.-DISPOSABLE METAL HANDLE SURGEONS SCALPELPrecision Surgical Industries, Inc.1986-10-24140
K863213KEISEI SCALPEL (STERILE AND NON-STERILE)Keisei Medical Industrial Co., Ltd.1986-09-02130
K854857SCALPEL, ONE-PIECE, DISPOSABLEMedelec Intl. Corp.1985-12-24190
K853103MCKNIFEMedical Dimensions1985-08-06140
K8517517-120, 7-130,7-140, 7-150,9-151 TO 168, 9-171 TO 1Artiberia1985-06-20560
K833467SURE-CUTDiverse Technologies, Inc.1984-01-271130
K834541H.R. JAKOBI SURG. INSTRUMENTS #9-SEC.48Imm Enterprises , Ltd.1984-01-27670
K830745ADT DISPOSABLE SCALPEL W/STAINLESS STEELLab Industries, Inc.1983-04-12350
K822893G.E.V. DISPOSABLE SCALPELSAscep, Inc.1982-10-22240
K822749PILLING DIAMOND KNIFENarco Scientific1982-10-06260
K820869DISPOSABLE #11 SCALPEL BLADE W/SHORTVan-Tec, Inc.1982-05-05370
K820730MICRO CISE DIAMOND SCALPELCooperVision, Inc.1982-04-09230
K813422SCALPELAbco Dealers, Inc.1982-01-05290
K811707AXICUT DISPOSABLE SCALPELNeonatal Corp.1981-07-20340
K800177I.M. BLADESInstrument Makar, Inc.1980-02-11140
K790259STERILE DISPOSABLE KNIFEIntermedics, Inc.1979-02-1370
K780998SCALPELIsolab, Inc.1978-07-27430

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