FDA applicant
Applied Medical Technologies
FDA records 24 decisions for Applied Medical Technologies (Independence, OH) from 1981 to 1998: 24 510(k) clearances. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and KGC (Tube, Gastro-Enterostomy). 6 recalls are linked to its devices.
FDA’s records also spell it “Applied Medical Technologies, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Applied Medical Technologies’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Applied Medical Technologies since 2007.
Recalls per year
1in 2015
Class I Class II/III not classified
Planning a device like Applied Medical Technologies’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) Report