FDA applicant

Hall-Tech

Mchenry, IL2 decisions1983–19840 recalls

FDA records 2 decisions for Hall-Tech (Mchenry, IL) from 1983 to 1984: 2 510(k) clearances. All are in product code EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.

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

How often FDA has decided Hall-Tech’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hall-Tech since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Hall-Tech”

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

Hall Surgical, Division of Zimmer, Inc. 8 Hall Laboratories, Inc. 2 Hall-Woodroof, Inc. 2 Hall Medical Laboratories 2 Hall/Mccollum Laboratories, Inc. 2

Hall-Tech

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hall-Tech”