Atlas FDA

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

Tyto Care , Ltd. — Predicate Candidate Screening

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

250 daysmedian FDA review time
330 days90th percentile
10clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K252844Tyto Insights for Wheeze Detection (with PCCP)Tyto Care , Ltd.2026-06-022670
DEN250014Tyto Insights for Eardrum Bulging DetectionTyto Care , Ltd.2026-03-173300
K252089Tyto Stethoscope (G3)Tyto Care , Ltd.2026-03-122530
K243567Tyto Insights for Rhonchi DetectionTyto Care , Ltd.2025-04-071400
K240555Tyto Insights for Crackles DetectionTyto Care , Ltd.2024-07-021250
K232237Tyto Insights for Wheeze DetectionTyto Care , Ltd.2023-12-131380
K221614TytoCare Lung Sounds AnalyzerTyto Care , Ltd.2023-02-242660
K190242Tyto ThermometerTyto Care , Ltd.2019-03-27490
K181612Tyto Stethoscope (OTC)Tyto Care , Ltd.2018-12-171810
K160401Tyto StethoscopeTyto Care , Ltd.2016-10-192500

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