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Loredan Biomedical, Inc.

United StatesFDA applicant, unverified

Devices
9

What Loredan Biomedical, Inc. makes

Loredan Biomedical, Inc. manufactures surgical instruments and systems for minimally invasive procedures, including retractors, tissue manipulation tools, and specialized sets for laparoscopic and endoscopic surgeries. Their portfolio includes products like the LIDO LIFT and LIDO V-TAK for tissue retraction and stabilization, as well as the LANE ONE system for surgical exposure. Additional offerings include the LIDO LINEA and LIDO ACTIVE series for precise tissue handling and the LIDO WORKSET for procedural efficiency.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance obtained through the 510(k) pathway. These products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

  • Lido(Tm) Lift Ref K880017

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

  • Lido V-Tak Ref K924512

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

  • Lido Linea Ref K903429

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

  • Lido Active Ref K871793

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

  • Lido(Tm) Workset Ref K880018

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

  • Lido(R) Linea Ref K924513

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

  • Lido Back Ref K861986

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

  • Lido Tm Active Back Ref K884487

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

  • Lane One Ref K832770

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

Frequently asked questions

How many devices does Loredan Biomedical, Inc. have in the registry?

The registry currently lists 9 devices for Loredan Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Loredan Biomedical, Inc.'s devices?

Among its 9 most recently registered devices, Loredan Biomedical, Inc. has devices listed in FDA 510(k) (9 devices).

What risk classes do Loredan Biomedical, Inc.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Loredan Biomedical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Loredan Biomedical, Inc. in the registry?

The most recently registered devices listed for Loredan Biomedical, Inc. include LIDO(TM) LIFT, LIDO V-TAK, LIDO LINEA and LIDO ACTIVE.

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