Atlas FDA

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

A.D.T. Lab Industries — Predicate Candidate Screening

21 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

28 daysmedian FDA review time
62 days90th percentile
21clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K812297A.D.T. PROCEDURES TRAYA.D.T. Lab Industries1981-09-28450
K801753ADT BONE MARROW BIOPSY-ASPIR. NEELDEA.D.T. Lab Industries1980-08-20230
K801754ADT BONE MARROW ASPIRATION NEEDLEA.D.T. Lab Industries1980-08-20230
K800418ADT DISPOSABLE THIN NEEDLE ASPIRATIONA.D.T. Lab Industries1980-04-28620
K800417ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDLA.D.T. Lab Industries1980-04-28620
K800412ROSENTHAL NEEDLE (DISP.) ADT BONE MARROWA.D.T. Lab Industries1980-04-28620
K800414ADT SOFT TISSUE BIOPSY TRAYA.D.T. Lab Industries1980-04-28620
K800409ADT BONE MARROW BIOPSY ASPIRATION TRAYA.D.T. Lab Industries1980-04-28620
K800410ADT BONE MARROW BIOPSY-ASPIRATION TRAYA.D.T. Lab Industries1980-04-28620
K800408ADT BONE MAR. BIO/ASP. TRAY W/NEEDLEA.D.T. Lab Industries1980-04-28620
K800411ASPIRATION TRAY W/FERRIS DISP. ILLINOISA.D.T. Lab Industries1980-04-28620
K800413FERRIS MODIFIED DISP. IL STERNAL-ILIACA.D.T. Lab Industries1980-03-25280
K800423ADT NERVE BLOCK TRAY(DISP.)A.D.T. Lab Industries1980-03-25280
K800415ADT MENGHINI TYPE SOFT TISSUE BIOPSYA.D.T. Lab Industries1980-03-25280
K800416ADT DISPOSABLE THIN NEEDLE(SKINNY CHIBA)A.D.T. Lab Industries1980-03-25280
K800421ADT PERITONEAL LAVAGE TRAY (DISP.)A.D.T. Lab Industries1980-03-25280
K800419ADT PERCUTANEOUS TRANSHEPATIC DISP. CHOLA.D.T. Lab Industries1980-03-25280
K800420ADT PERCUTANEOUS NON-DISP. NEEDLEA.D.T. Lab Industries1980-03-25280
K800422ADT MINI PERITONEAL LAVAGE KITA.D.T. Lab Industries1980-03-12150
K800406FERRIS BONE MARROW BIOPSY-ASPIR. NEEDLEA.D.T. Lab Industries1980-03-12150
K800407FERRIS BONE MARROW -NEEDLE-(DISPOSABLE)A.D.T. Lab Industries1980-03-12150

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