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The Buckeye Cellulose Corp.

United StatesFDA applicant, unverified

Devices
18

What The Buckeye Cellulose Corp. makes

The Buckeye Cellulose Corp. manufactures single-use surgical drapes, including reinforced and gown variants, as well as craniotomy sheets designed for sterile barrier applications. Their product line also includes x-ray detectable lap sponges, boundary tubing holders, and odor-masking agents for medical contents and obstetric procedures. These items are intended for use in surgical settings to maintain sterility and reduce contamination risks.

The company’s devices are regulated under FDA Class I and Class II classifications, with many products requiring 510(k) clearance. Their products are listed in the FDA’s 510(k) registry, and the company is based in the United States.

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

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  • Boundary Surgical Drape Ref K812962

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

  • Contain X-Ray Detectable Lap Sponge Ref K801768

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

  • Boundary Single-Use Craniotomy Sheet Ref K820758

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

  • Boundary Single-Use Drapes Ref K813450

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

  • Boundary Reinforced Or Gown Ref K811958

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

  • Boundary Process Change Ref K821564

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

  • Boundary Ref K820116

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

  • Odor Masking Agent For Contents Of All Ref K801025

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

  • Bondary Single-Use Or Gown Ref K813390

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

  • Odor Masking Agent In Boundary Obstetri. Ref K801024

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

  • Boundary Tubing Holders Ref K810888

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

  • Boundary Process Change Ref K812738

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

  • Irradiated Boundary Devices Ref K803158

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

  • Boundary Single-Use Gowns Ref K822925

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

  • Patient Underpad Ref K813263

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

  • Boundary Drape Tape Ref K813277

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

  • Arrirm Scrub Brush/Sponge Ref K823173

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

  • Boundary Sterilization Wrap Ref K811819

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

Rows 1-18 of 18

Frequently asked questions

How many devices does The Buckeye Cellulose Corp. have in the registry?

The registry currently lists 18 devices for The Buckeye Cellulose Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Buckeye Cellulose Corp.'s devices?

Among its 18 most recently registered devices, The Buckeye Cellulose Corp. has devices listed in FDA 510(k) (18 devices).

What risk classes do The Buckeye Cellulose Corp.'s devices fall under?

Among its 18 most recently registered devices, the classes recorded for The Buckeye Cellulose Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Buckeye Cellulose Corp. in the registry?

The most recently registered devices listed for The Buckeye Cellulose Corp. include BOUNDARY SURGICAL DRAPE, CONTAIN X-RAY DETECTABLE LAP SPONGE, BOUNDARY SINGLE-USE CRANIOTOMY SHEET and BOUNDARY SINGLE-USE DRAPES.

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