Atlas FDA

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

LYN · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K950995SENSICARE SYNTHETIC, SURGICAL GLOVE LINERBd Becton Dickinson Vacutainer Systems Preanalytic1995-06-281170
K897143VERA 103Madsen North America, Inc.1990-04-271210
K880259VISUAL REINFORCE. AUDIO CASSETTE UNIT: BASIC & ADVColorado Hearing Systems, Inc.1989-04-034370

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