FDA applicant

Aesculap Instruments Corp.

Mchenry, IL13 decisions1977–19900 recalls

FDA records 13 decisions for Aesculap Instruments Corp. (Mchenry, IL) from 1977 to 1990: 13 510(k) clearances. Most are in product codes DZA (Drill, Dental, Intraoral) and LYS (Bone Mill). 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 Aesculap Instruments Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aesculap Instruments Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Aesculap”

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

Aesculap, Inc. 219 Aesculap Implant Systems, LLC 51 Aesculap Implant System, Inc. 18 Aesculap-Meditec North America 6 Aesculap Implants Systems, LLC 4 Aesculap-Meditec GmbH 3

Aesculap Instruments Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Aesculap”