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Cedar Surgical, Inc.

United StatesFDA applicant, unverified

Devices
17

What Cedar Surgical, Inc. makes

Cedar Surgical, Inc. manufactures surgical instruments and orthopedic tools, including retractors, dissecting hooks, depth gauges, periosteal elevators, protective retractors, and bone impactors. Their portfolio also covers specialized orthopedic accessories like the Raylor Fusion Funnel and mallet, as well as an upper-chest-support cushion for surgical procedures. The company produces mini-probes and drill stops for precision orthopedic applications.

The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. These instruments are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue17

Newest first, rows 1-17 of 17

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  • Raylor Fusion Funnel Ref K872281

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

  • Raylor(Tm) Mallet Ref K864422

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

  • Upper-Chest-Support Cushion For Operations In Sitt Ref K853800

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

  • Bone Impactors Ref K853798

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

  • Raylor(Tm) Dissecting Hook Ref K864425

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

  • Cedar(Tm) Retractor Ring Ref K873691

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

  • Raylor(Tm) Depth Gauge Ref K864426

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

  • Raylor(Tm) Periosteal Elevators Ref K864421

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

  • Raylor(Tm) Protective Retractor Ref K864424

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

  • Raylor Mini-Probe Ref K863416

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

  • Raylor(Tm) Drill Stop Ref K873692

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

  • Raylor Bone Impactors Ref K863415

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

  • Kneeling Attachment & Cushioned Face Rest Sys For Ref K853797

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

  • Raylor(Tm) Osteotomes Ref K864423

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

  • Cedar(Tm) Pelvic Cushion Ref K873690

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

  • Raylor Retractors Ref K853796

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

  • Neurosurgical Headrest Ref K853799

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

Rows 1-17 of 17

Frequently asked questions

How many devices does Cedar Surgical, Inc. have in the registry?

The registry currently lists 17 devices for Cedar Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cedar Surgical, Inc.'s devices?

Among its 17 most recently registered devices, Cedar Surgical, Inc. has devices listed in FDA 510(k) (17 devices).

What risk classes do Cedar Surgical, Inc.'s devices fall under?

Among its 17 most recently registered devices, the classes recorded for Cedar Surgical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cedar Surgical, Inc. in the registry?

The most recently registered devices listed for Cedar Surgical, Inc. include RAYLOR FUSION FUNNEL, RAYLOR(TM) MALLET, UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT and BONE IMPACTORS.

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