Atlas FDA

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

Ideal Life, Inc. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K132180IDEAL LIFE GLUCO-MANAGER BLOOD GLUCOSE MONITORING SYSTEMIdeal Life, Inc.2014-06-253450
K080538IDEAL LIFE POD (MODEL ILP 0001)Ideal Life, Inc.2008-07-031280
K060504IDEAL LIFE BP-MANAGER, MODEL BPM 0001; IDEAL LIFE POD, MODELIdeal Life, Inc.2006-03-14150

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