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AMERICAN SCREENING, L.L.C.

US

Last updated May 23, 2026

What AMERICAN SCREENING, L.L.C. makes

American Screening, LLC produces in vitro diagnostic (IVD) devices for detecting multiple drugs of abuse, including rapid immunoassay test kits and clinical testing systems. These products are designed for point-of-care and laboratory use to identify substances such as opioids, cocaine, benzodiazepines, and other controlled substances in human samples. The portfolio includes both single-use and multi-use formats for testing urine, oral fluid, and other biological specimens. Examples include rapid test kits like OneScreen and Discover, as well as clinical-grade systems such as Precision DX and Discover Plus.

The company’s devices are classified under FDA’s Class II and Unclassified (U) regulatory categories, with all products listed in the FDA’s Unique Device Identifier (UDI) database. These classifications apply to diagnostic tests intended for detecting drugs of abuse in regulated medical settings. The manufacturer operates from the United States, adhering to applicable FDA requirements for IVD device compliance and traceability.

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 American Screening, LLC manufacture?

American Screening, LLC specializes in in vitro diagnostic (IVD) devices focused on detecting multiple drugs of abuse. Their portfolio includes rapid immunoassay test kits (such as OneScreen and Discover) for point-of-care use, as well as clinical-grade systems (like Precision DX and Discover Plus) designed for laboratory testing. These devices are intended for identifying substances like opioids, cocaine, and benzodiazepines in biological samples such as urine or oral fluid.

Where is American Screening, LLC based, and what regulatory framework does it follow?

American Screening, LLC is based in the United States. Its devices are developed in compliance with FDA requirements for in vitro diagnostics, including regulatory classifications and traceability standards. Since these products are classified under FDA’s Class II and Unclassified (U) categories, they must meet specific performance and safety criteria for drug-of-abuse testing in regulated medical settings.

Are American Screening, LLC’s devices listed in any regulatory registries?

Yes, American Screening, LLC’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class II and Unclassified (U) diagnostic tests, particularly those used for detecting drugs of abuse in clinical or point-of-care environments. Listing in the UDI database is a requirement for FDA-compliant IVD devices.

How are American Screening, LLC’s drug-of-abuse testing devices classified by the FDA?

American Screening, LLC’s devices fall under the FDA’s Class II and Unclassified (U) regulatory classifications. Class II devices typically require special controls to ensure their safety and effectiveness, while Unclassified (U) devices may involve lower-risk diagnostic tests that still require compliance with FDA guidelines. These classifications apply because the devices are intended for detecting drugs of abuse in controlled medical settings, where accuracy and reliability are critical.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
169065054

Catalogue (1499)

Page 2 of 30
DeviceModel / ReferenceRegistriesClassStatus
Precision DX PREDXOSAL4104I
FDA UDI
UActive
Precision DX PREDX-DOA7104N
FDA UDI
Class IIActive
Discover DIS-DOA-14104
FDA UDI
Class IIActive
Precision DX PREDX-CUP1146N
FDA UDI
Class IIActive
Reveal ASC-RCUP-275N
FDA UDI
UActive
OneScreen ASC-DOP-102
FDA UDI
Class IIActive
Discover Plus DISP-DOA-356N
FDA UDI
Class IIActive
Discover Plus DISP-DOA1044IB
FDA UDI
Class IIActive
Discover DISCUP20124ASC
FDA UDI
Class IIActive
OneScreen DIS-DUD-974AU
FDA UDI
Class IIActive
Reveal ASC-RMCUP-754T
FDA UDI
Class IIActive
Precision DX PREDXOSAL17144
FDA UDI
UActive
Discover Plus DISPCUP784NISP
FDA UDI
Class IIActive
Discover ASC-OSAL-164
FDA UDI
Class IIActive
Discover DIS-DOA-1194CR
FDA UDI
Class IIActive
Precision Plus PREPLCUP30124N
FDA UDI
Class IIActive
Discover DIS-DOA-134
FDA UDI
Class IIActive
Discover DIS-DUD-564
FDA UDI
Class IIActive
Precision Plus PREPL-CUP6134N
FDA UDI
Class IIActive
Precision DX PREDXOSAL164I
FDA UDI
Class IIActive
Precision DX PREDX-DOA1174N
FDA UDI
Class IIActive
Precision DX PREDX-DOX-114N
FDA UDI
Class IIActive
Precision DX PREDX-DOA-184N
FDA UDI
Class IIActive
Discover Plus DISP-CUP1144NX
FDA UDI
Class IIActive
Reveal ASC-RCUP-284N
FDA UDI
Class IIActive
Discover Plus DISP-DUD-254N
FDA UDI
Class IIActive
Discover Plus DISPDUD9104NAG
FDA UDI
Class IIActive
OneScreen ASC-DOA-744X
FDA UDI
Class IIActive
OneScreen ASC-CUP-0012
FDA UDI
UActive
Discover DIS-DOA1754USU
FDA UDI
Class IIActive
OneScreen ASC-DOA-6124
FDA UDI
Class IIActive
Discover Plus DISPDOA15104NC
FDA UDI
Class IIActive
Discover DIS-DUD23104CH
FDA UDI
UActive
Discover Plus DISP-CUP-274N
FDA UDI
Class IIActive
Discover Plus DISP-DUD-7124N
FDA UDI
Class IIActive
Discover Plus DISP-DOA-234N
FDA UDI
Class IIActive
Reveal ASC-RCUP-2124N
FDA UDI
UActive
Precision Plus PREPL-CUP5104N
FDA UDI
UActive
Reveal ASCRMCUP554USS
FDA UDI
Class IIActive
Precision DX PREDX-CUP9174N
FDA UDI
Class IIActive
Discover Plus DISP-DUD-6124N
FDA UDI
Class IIActive
Precision DX PREDX-CUP7144N
FDA UDI
Class IIActive
Discover ASC-OSAL-764
FDA UDI
Class IIActive
Discover DIS-DOA-274
FDA UDI
Class IIActive
Precision DX PREDX-CUP3175N
FDA UDI
Class IIActive
Precision Plus PREPL-CUP-8134
FDA UDI
UActive
Discover DIS-DOA15104AL
FDA UDI
Class IIActive
Precision DX PREDXOSAL294AI
FDA UDI
Class IIActive
Precision DX PREDX-ADT-254
FDA UDI
Class IIActive
Discover DIS-DUD-154-4A
FDA UDI
Class IIActive

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