FDA applicant

Adri/Technam

Park Forest, IL3 decisions1991–20000 recalls

FDA records 3 decisions for Adri/Technam (Park Forest, IL) from 1991 to 2000: 3 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and KGN (Wound Dressing With Animal-Derived Material (S)). 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 hospital panel, where it files most

How often FDA has decided Adri/Technam’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Adri/Technam since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Adri/Technam by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Adri/Technam’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 “Adri/Technam”

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

Adri 6

Adri/Technam

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Adri/Technam”