FDA applicant
Triad Life Sciences, Inc.
FDA records 4 decisions for Triad Life Sciences, Inc. (Memphis, TN) from 2020 to 2022: 4 510(k) clearances. All are in product code KGN (Wound Dressing With Animal-Derived Material (S)). Since 2016 its 510(k)s took a median of 308 days from receipt to decision, against 246 for FDA’s reviews in the same codes and years. Its devices cite 4 predicates, 2 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Triad Life Sciences, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2022
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2020.
Planning a device like Triad Life Sciences, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Triad”
FDA records each applicant name separately; these may or may not be the same firm.