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Concord Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
42

What Concord Laboratories, Inc. makes

Concord Laboratories, Inc. manufactures prefilled pulsator syringes for arterial blood sampling, epidural and catheterization trays, and specialized blood gas sampling kits. Their portfolio includes arterial blood sampling syringes, subcutaneous tunneling needles, and heparin vaporization devices, as well as disposable trays for medical procedures. The company also produces blood sampling accessories, such as arterial blood sampling kits and catheterization trays with conduction catheters.

The company’s devices are regulated under FDA Class I, Class II, and Unclassified (U) classifications, with many listed via the 510(k) pathway. Products are distributed in the United States, where the manufacturer is based.

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

Catalogue42

Newest first, rows 1-42 of 42

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  • Prefilled Pulsator Syringe Ref K811009

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

  • Epidural Trays Ref K842095

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

  • Syringe, Blood Sampling, Arterial, #4015 Ref K770852

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

  • Arterial Blood Sampling Kits Ref K841486

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

  • Tray, Blood Sampling (Pulsator Ii) Ref K760086

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

  • Sani Catch Ba Ref K833814

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

  • Tray, Catheterization W/ Catheter Ref K760128

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

  • Spring Guide Catheter Anesthesia Conduction Cath Ref K854601

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

  • Tray, Blood Gas, Arterial, #4014 Ref K770850

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

  • Subcutaneous Tunneling Needles & Handles Ref K854327

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

  • Pulsator Arterial Blood Sampling Syrin Ref K833582

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

  • Vaporized Heparin Ref K840987

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

  • Subclavian Tray Ref K780419

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

  • Drainage Bag, 4000 Ml. Ref K770557

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

  • Universal Tray Ref K770496

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

  • Catheter, Silicone Coated Ref K772218

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

  • Collector, Sani-Catch, No. 1010 Ref K770672

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

  • Tracheobronchial Suction Catheter, Cat. No. 6110 Ref K864535

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

  • Prefilled Pulsator Syringe Ref K810995

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

  • Concord Care Tray Ref K862039

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

  • Mid-Stream Urine Collection Sets Ref K840709

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

  • No Pour Basin Ref K840988

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

  • Drainage Unit, Combination Ref K770497

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

  • Collector, Sani-Catch, No. 1014 Ref K770673

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

  • Urethral Tray W/Out Cahteter, 7650 Ref K771104

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

  • Urethral Tray W/Catheter, 7750 Ref K771103

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

  • Catheteo Care Tray #0242 Ref K771673

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

  • Epidural Syringe Ref K832778

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

  • Syringe, Blood Sampling, Arterial, #4016 Ref K770851

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

  • Blood Gas Tray #4024 Ref K771667

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

  • Catheter Suction Tracheobronchial Ref K801814

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

  • Bag, Urine Collection, Closed System Ref K760105

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

  • Tray, Blood Gas, Cat. No. 4010 Ref K770361

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

  • Regional Anesthesia Trays Ref K851134

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

  • Tray, Catheterization W/O Catheter Ref K760127

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

  • Meconium Suction Catheter Ref K871825

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

  • Alcohol Swabs Ref K833993

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

  • Prefilled Pulsator Syringe Ref K840986

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

  • Acetone Alcohol Swabs Ref K833936

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

  • Clamp, Disposable Ref K782090

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

  • Dri-Vent Arterial Blood Sampling Kit Ref K883840

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

  • Basin, Sterile (#3200) Ref K760085

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

Rows 1-42 of 42

Frequently asked questions

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

The registry currently lists 42 devices for Concord Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Concord Laboratories, Inc.'s devices?

Among its 42 most recently registered devices, Concord Laboratories, Inc. has devices listed in FDA 510(k) (42 devices).

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

Among its 42 most recently registered devices, the classes recorded for Concord Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Concord Laboratories, Inc. include PREFILLED PULSATOR SYRINGE, EPIDURAL TRAYS, SYRINGE, BLOOD SAMPLING, ARTERIAL, #4015 and ARTERIAL BLOOD SAMPLING KITS.

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