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Acacia, Inc.

United StatesFDA applicant, unverified

Devices
17

What Acacia, Inc. makes

Acacia, Inc. manufactures single-use and reusable medical devices for fluid administration, sampling, and drug delivery, including spring-loaded syringes, syringe tip adaptors, and luer lock transfer pins. Their portfolio also covers blood sampling sets, ophthalmic dropper bottles, and tandem intravenous sets, as well as vented plastic needles and tamper-proof caps. The company produces piston syringes and specialized components like blunt cannulas for safer fluid transfer.

Acacia’s devices are regulated under FDA’s Class I and Class II classifications, with many listed via the 510(k) pathway. The products are intended for use in the US and comply with applicable medical device regulations. The company is headquartered in the United States.

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

Catalogue17

Newest first, rows 1-17 of 17

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  • Spring Loaded Syringe Ref K931095

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

  • Syringe Tip Adaptor Ref K894217

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

  • Intopo Ref K894206

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

  • Luer Lock Transfer Pin Ref K901063

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

  • Blood Sampling Set Ref K103165

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

  • Acacia Piston Syringe Ref K092986

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

  • Ophthalmic Dropper Bottles Ref K850962

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

  • Cap, Tamper Proof Plastic Ref K782113

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

  • Tandem Sets I.V. Ref K850757

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

  • Acacias Pharm/Pump Ref K912771

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

  • Flow-Eze Blunt Cannula (1999BC) Ref K972538

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

  • Flow Ease(Plastic Vented Needle) Ref K853212

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

  • Enteral Nutrition Warmer Ref K122449

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

  • Medi-Sis Syringe Infusion System Ref K111381

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

  • Extension Set with BD Q-Syte Luer Access Split Septum Ref K142527

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

  • Pharmulator Ref K896990

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

  • Hi Volume Pumping Chamber Ref K802561

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

Rows 1-17 of 17

Frequently asked questions

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

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

Which registries list Acacia, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Acacia, Inc. include SPRING LOADED SYRINGE, SYRINGE TIP ADAPTOR, INTOPO and LUER LOCK TRANSFER PIN.

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