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Lsl Industries, Inc.

US

Last updated May 23, 2026

What Lsl Industries, Inc. makes

The company manufactures single-use and reusable surgical kits, including medicated and non-medicated general surgical procedure kits, suture kits, and urethral catheterization support kits for urinary drainage. It also produces tracheostomy kits, single-use surgical drapes, and non-powdered, non-antimicrobial nitrile examination gloves.

These products are regulated as Class I and Class II devices under FDA guidelines and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Lsl Industries, Inc. manufacture?

Lsl Industries, Inc. specializes in surgical and procedural medical devices, primarily focused on single-use and reusable kits. Their portfolio includes medicated and non-medicated general surgical procedure kits, suture kits (both medicated and non-medicated), urethral catheterization support kits for urinary drainage, tracheostomy kits, single-use surgical drapes, and nitrile examination/treatment gloves that are non-powdered and non-antimicrobial. These devices are designed to support a range of surgical and clinical procedures.

Where is Lsl Industries, Inc. based, and how does that affect its regulatory oversight?

Lsl Industries, Inc. is based in the United States, which means its devices are subject to FDA regulations. Since the company manufactures products like surgical kits and gloves, these fall under FDA’s classification system, where they are designated as either Class I or Class II devices. The FDA’s jurisdiction ensures these products meet safety, performance, and labeling requirements before they enter the market.

Which regulatory registries or databases list Lsl Industries, Inc.’s devices?

Lsl Industries, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a standardized identifier to medical devices to improve tracking, reduce medical errors, and enhance transparency in the healthcare supply chain. This listing helps healthcare providers and regulators verify device details, such as manufacturer information and regulatory classification.

How are Lsl Industries, Inc.’s devices classified under FDA regulations?

Lsl Industries, Inc.’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and may only require general controls like good manufacturing practices. Class II devices involve a higher level of risk and may require additional controls, such as performance standards or post-market surveillance, to ensure their safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with.

What distinguishes Lsl Industries, Inc.’s single-use devices from their reusable ones?

Lsl Industries, Inc. produces both single-use and reusable surgical kits, with the primary distinction being their intended lifespan and sterilization requirements. Single-use devices, such as tracheostomy kits and surgical drapes, are designed for one-time use and disposal to minimize infection risks. Reusable devices, like some general surgical procedure kits or suture kits, are intended to be sterilized and used multiple times, requiring adherence to strict cleaning and sterilization protocols to maintain safety and efficacy.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
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LinkedIn
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Email
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Catalogue (344)

Page 3 of 7
DeviceModel / ReferenceRegistriesClassStatus
Lsl Healthcare 3323B
FDA UDI
Class IIActive
Lsl Healthcare 1008
FDA UDI
Class IActive
Lsl Healthcare 2532B
FDA UDI
Class IActive
Lsl Healthcare 7481
FDA UDI
Class IIActive
Lsl Healthcare 3424
FDA UDI
Class IIActive
Lsl Healthcare 2110I
FDA UDI
Class IActive
Lsl Healthcare 3424B
FDA UDI
Class IIActive
Lsl Healthcare 3439
FDA UDI
Class IIActive
Lsl Healthcare 7512
FDA UDI
Class IActive
Lsl Healthcare 7184
FDA UDI
Class IIActive
Lsl Healthcare 2101
FDA UDI
Class IActive
Lsl Healthcare 7105
FDA UDI
Class IActive
Lsl Healthcare 7196
FDA UDI
Class IActive
Lsl Healthcare 3264
FDA UDI
Class IIActive
Lsl Healthcare 7128-0524
FDA UDI
Class IActive
Lsl Healthcare 3013A
FDA UDI
Class IIActive
Lsl Healthcare 7544
FDA UDI
Class IActive
Lsl Healthcare 3198B
FDA UDI
Class IIActive
Lsl Healthcare 2310F
FDA UDI
Class IActive
Lsl Healthcare 3296
FDA UDI
Class IIActive
Lsl Healthcare 8441-1
FDA UDI
Class IActive
Lsl Healthcare 3174B
FDA UDI
Class IIActive
Lsl Healthcare 7109
FDA UDI
Class IActive
Lsl Healthcare 2923ACP
FDA UDI
Class IActive
Lsl Healthcare 2557CP
FDA UDI
Class IActive
Lsl Healthcare 2994
FDA UDI
Class IActive
Lsl Healthcare 7508
FDA UDI
Class IActive
Lsl Healthcare 2991A
FDA UDI
Class IIActive
Lsl Healthcare 7103P
FDA UDI
Class IActive
Lsl Healthcare 7528
FDA UDI
Class IIActive
Lsl Healthcare 7128
FDA UDI
Class IActive
Lsl Healthcare 2345
FDA UDI
Class IIActive
Lsl Healthcare 3439B
FDA UDI
Class IIActive
Lsl Healthcare 3135
FDA UDI
N/AActive
Lsl Healthcare 7632
FDA UDI
Class IIActive
Lsl Healthcare 3330A-1
FDA UDI
Class IIActive
Lsl Healthcare 3527
FDA UDI
Class IIActive
Lsl Healthcare 2923CP
FDA UDI
Class IIActive
Lsl Healthcare 1558
FDA UDI
Class IActive
Lsl Healthcare 2709
FDA UDI
Class IIActive
Lsl Healthcare 2699A
FDA UDI
Class IActive
Lsl Healthcare 3040
FDA UDI
Class IIActive
Lsl Healthcare ADM1022
FDA UDI
Class IActive
Lsl Healthcare 3545-1
FDA UDI
Class IIActive
Lsl Healthcare 2310I
FDA UDI
Class IActive
Lsl Healthcare 3464OR
FDA UDI
Class IIActive
Lsl Healthcare B4019-012-000
FDA UDI
Class IActive
Lsl Healthcare 3042
FDA UDI
Class IIActive
Lsl Healthcare 7165
FDA UDI
Class IActive
Lsl Healthcare 6279
FDA UDI
Class IActive

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