510(k) Report

FDA applicant

Mend Technologies, Inc.

Dallas, TX3 decisions1988–19930 recalls

FDA records 3 decisions for Mend Technologies, Inc. (Dallas, TX) from 1988 to 1993: 3 510(k) clearances. Most are in product codes HEB (Tampon, Menstrual, Unscented) and BWN (Table And Attachments, Operating-Room). 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 Mend Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mend Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HEBTampon, Menstrual, Unscented1decision
  • BWNTable And Attachments, Operating-Room1decision
  • JEATable, Surgical With Orthopedic Accessories, Ac-Powered1decision

What has FDA decided for it lately?

  • K924094Mend ApcMend Technologies, Inc. · 1993
  • K883867Cervical Biopsy InstrumentMend Technologies, Inc. · 1988
  • K884558Iop Adjustable StirrupMend Technologies, Inc. · 1988

All 3 as Mend Technologies, Inc. →