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JACKSON MEDICAL LLC

US

Last updated May 31, 2026

What JACKSON MEDICAL LLC makes

Jackson Medical LLC manufactures single-use laparoscopic access cannula seals designed to provide a barrier during minimally invasive surgical procedures. These devices are intended to reduce the risk of contamination and maintain sterility within the surgical site during laparoscopic operations.

The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Jackson Medical LLC manufacture?

Jackson Medical LLC specializes in single-use laparoscopic access cannula seals. These devices are specifically designed to create a barrier during minimally invasive surgical procedures, helping to reduce contamination risks and maintain sterility within the surgical site. The primary focus is on improving safety in laparoscopic surgeries.

Where is Jackson Medical LLC based?

Jackson Medical LLC is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

How are the devices manufactured by Jackson Medical LLC classified under regulatory standards?

The devices produced by Jackson Medical LLC fall under Class I classification according to FDA regulations. This classification is typically assigned to devices posing minimal risk to patients, such as single-use items like laparoscopic access cannula seals, which are intended for straightforward, low-risk applications in surgical settings.

Are Jackson Medical LLC’s devices listed in any regulatory registries?

Yes, Jackson Medical LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for medical devices, allowing healthcare providers, regulators, and other stakeholders to identify and verify the specific products under the manufacturer’s portfolio.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
678-856-7454
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
080935024

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
GloShield 16-2001
FDA UDI
Class IActive
GloShield 17-2001
FDA UDI
Class IActive

Related Companies

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