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SLANTED ADAPTOR LLC

US

Last updated May 24, 2026

What SLANTED ADAPTOR LLC makes

Slanted Adaptor LLC manufactures manual syringe-loaded medication and vaccine injectors designed for professional use. These devices are intended for single-dose administration of liquids from syringes, ensuring precise delivery in clinical or medical settings.

The company’s products fall under FDA Class I medical devices 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 Slanted Adaptor LLC manufacture?

Slanted Adaptor LLC specializes in manual syringe-loaded medication and vaccine injectors for professional use. These devices are designed to administer single doses of liquids from syringes with precision, typically in clinical or medical environments. The focus is on ensuring accurate delivery of medications or vaccines in controlled settings.

Where is Slanted Adaptor LLC based?

Slanted Adaptor 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.

Which regulatory registries or databases list Slanted Adaptor LLC’s devices?

Slanted Adaptor LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance with regulatory requirements.

How are Slanted Adaptor LLC’s devices classified by regulatory authorities?

Slanted Adaptor LLC’s devices fall under FDA Class I medical device classification. Class I devices are generally considered to pose the lowest risk and often require minimal regulatory oversight, though compliance with manufacturing and labeling standards remains mandatory.

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

Information

Country
US
Address
—
LinkedIn
—
Facebook
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Phone
5625462811
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
074078018

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
SyringePro 10mLNSSU
FDA UDI
Class IActive

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