510(k) Report

FDA applicant

Hinson and Hale Medical Technologies, Inc.

Austin, TX2 decisions2010–20100 recalls

FDA records 2 decisions for Hinson and Hale Medical Technologies, Inc. (Austin, TX) in 2010: 2 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and KKX (Drape, Surgical, Antimicrobial). 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 Hinson and Hale Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2010

2010: 2
2010high 2 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Hinson and Hale Medical Technologies, Inc. by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FRGWrap, Sterilization1decision
  • KKXDrape, Surgical, Antimicrobial1decision

What has FDA decided for it lately?

  • K102783Hinson & Hale Medical Technologies Infused (R) Polyester WrappersHinson and Hale Medical Technologies, Inc. · 2010
  • K094016Next Generation Infused (R) or Towel (Hemed), Next Generation Infused (R) or Towel (with Binding) Model…Hinson and Hale Medical Technologies, Inc. · 2010

All 2 as Hinson and Hale Medical Technologies, Inc. →