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Aesculap Instruments Corp.

United StatesFDA applicant, unverified

Devices
13

What Aesculap Instruments Corp. makes

Aesculap Instruments Corp. manufactures surgical instruments and dental devices, including bone milling tools, aneurysm clips, and dental handpieces, as well as prosthetic implants like the Resurface ProShesis and dental prostheses (ProteGraft DV series). The company also produces orthopedic and soft-tissue retraction systems, such as the Robotrac Retractor Arm, along with specialized surgical accessories like valve strippers, suction regulators, and scalp clips. Dental-specific tools include drills, burrs, and container systems for surgical instruments.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with many products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

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  • Protegraft Dv 1500, 1900 & Low Por, Unigraft Dv Ref K890182

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Resurface Proshesis Ref K781343

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Container System Ref K792558

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Drill, Dental Ref K801887

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Insitucat Valve Stripper Ref K885046

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Yasargil Aneurysm Clips Ref K772200

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Robotrac (Tm) Retractor Arm Ref K893121

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Handpiece, Dental Ref K801888

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Caspar Scalp Clip, Applier Ref K890443

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cerullo Suction Regulator Ref K880704

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Burr, Dental Ref K801886

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Aesculap Bone Mill Ref K860016

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Elan-E Disposable Drape Ref K884057

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-13 of 13

Frequently asked questions

How many devices does Aesculap Instruments Corp. have in the registry?

The registry currently lists 13 devices for Aesculap Instruments Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aesculap Instruments Corp.'s devices?

Among its 13 most recently registered devices, Aesculap Instruments Corp. has devices listed in FDA 510(k) (13 devices).

What risk classes do Aesculap Instruments Corp.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Aesculap Instruments Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Aesculap Instruments Corp. in the registry?

The most recently registered devices listed for Aesculap Instruments Corp. include PROTEGRAFT DV 1500, 1900 & LOW POR, UNIGRAFT DV, RESURFACE PROSHESIS, CONTAINER SYSTEM and DRILL, DENTAL.

Generated automatically from registry data and not verified by a human reviewer.