Atlas FDA

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

Medtech Industries, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K910451CARD GUARD, MODEL CG-2000AMedtech Industries, Inc.1991-06-101290
K910450CARD GUARD-3000 ECG TELEPHONE ADAPTERMedtech Industries, Inc.1991-05-07950
K842819HOOK PUNCH FORCEPS FOR ARTHROSCOPYMedtech Industries, Inc.1984-08-14260
K842820ARTHROSCOPY KNIVESMedtech Industries, Inc.1984-08-14260

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