Atlas FDA

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

Today'S Machining & Design, Inc. — Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K853604ACE-KYLE DYE INJECTION NEEDLE P/N 14082Today'S Machining & Design, Inc.1985-11-12760
K834108NEEDLE BENDER TX8225Today'S Machining & Design, Inc.1984-03-121040
K823676DISC NEEDLE SET #TX-8220Today'S Machining & Design, Inc.1983-01-09330
K823675FRONING GUIDANCE SYSTEM #TX-8200Today'S Machining & Design, Inc.1983-01-05290

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