510(k) Report

FDA applicant

Medin Corp.

Wallington, NJ5 decisions1977–19930 recalls

FDA records 5 decisions for Medin Corp. (Wallington, NJ) from 1977 to 1993: 5 510(k) clearances. Most are in product codes GAD (Retractor) and FLE (Sterilizer, Steam). 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 Medin Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medin Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medin Corp. 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?

  • GADRetractor3decisions
  • FLESterilizer, Steam1decision
  • FRGWrap, Sterilization1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K833343Sterilization ContainerMedin Corp. · 19832cite it

What has FDA decided for it lately?

  • K921017Hargis SR2 Self-Retraction SystemMedin Corp. · 1993
  • K921020Hargis Self Retraction SystemMedin Corp. · 1993
  • K921019Hargis Rectal Self Retration SystemMedin Corp. · 1993
  • K833343Sterilization ContainerMedin Corp. · 1983
  • K761032Cradling SystemMedin Corp. · 1977

All 5 as Medin Corp. →

Other applicant names beginning “Medin”

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

Medin Tech 1