FDA applicant

Penn-Med Technology, Inc.

Mchenry, IL2 decisions1985–19850 recalls

FDA records 2 decisions for Penn-Med Technology, Inc. (Mchenry, IL) in 1985: 2 510(k) clearances. All are in product code EJL (Bur, Dental). 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, dental panel, where it files most

How often FDA has decided Penn-Med Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Penn-Med Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Penn-Med”

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

Penn Medical Devices, Inc. 8 Penn-Tech Laboratories 1

Penn-Med Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Penn-Med”