FDA applicant

Bemiss-Jason Corp., Triad Medical Div.

Waynesville, NC1 decision1997–19970 recalls

FDA records 1 decision for Bemiss-Jason Corp., Triad Medical Div. (Waynesville, NC) in 1997: 1 510(k) clearance. All are in product code FYA (Gown, Surgical). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Bemiss-Jason Corp., Triad Medical Div.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bemiss-Jason Corp., Triad Medical Div. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bemiss-Jason Corp., Triad Medical Div. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Bemiss-Jason Corp., Triad Medical Div.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Bemiss-Jason”

FDA records each applicant name separately; these may or may not be the same firm.

Bemiss Jason Corp. 1

Bemiss-Jason Corp., Triad Medical Div.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bemiss-Jason”