Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
169065054

Catalogue (1499)

Page 15 of 30
DeviceModel / ReferenceRegistriesClassStatus
Discover DIS-CUP21104SP
FDA UDI
Class IIActive
Discover DIS-DOA274AL
FDA UDI
Class IIActive
Discover Plus DISP-DUD-5124N
FDA UDI
Class IIActive
Discover Plus DISPDUD26104US
FDA UDI
UActive
Precision DX PREDX-DOA-116N
FDA UDI
Class IIActive
Precision DX PREDX-U-VACL
FDA UDI
Class IIActive
Discover Plus DISP-CUP-564SN
FDA UDI
Class IIActive
Precision Plus PREPL-DUD-268N
FDA UDI
Class IIActive
Precision Plus PREPL-CUP1354N
FDA UDI
Class IIActive
Discover DIS-DMT-114
FDA UDI
Class IIActive
Discover ASC-SAL-264
FDA UDI
Class IIActive
Precision DX PREDX-CUP8104N
FDA UDI
Class IIActive
Discover DIS-CUP-274
FDA UDI
Class IIActive
Precision PRES-SAL-164A
FDA UDI
Class IIActive
Precision DX PREDX-DOA60124
FDA UDI
Class IIActive
Discover Plus DISP-DOA-664N
FDA UDI
Class IIActive
Precision DX PREDX-DOA-124N
FDA UDI
Class IIActive
Discover Plus DISPCUP22124NC
FDA UDI
Class IIActive
Discover Plus DISPDUD22124NF
FDA UDI
Class IIActive
Precision DX PREDX-DOA2114N
FDA UDI
Class IIActive
OneScreen ASC-DOA-5114
FDA UDI
Class IIActive
Discover Plus DISP-DUD2084OV
FDA UDI
Class IIActive
Precision DX PREDX-DOA50124
FDA UDI
Class IIActive
Precision Plus PREPL-DUD1145
FDA UDI
Class IIActive
Discover Plus DISP-DOA434NPT
FDA UDI
Class IIActive
Precision DX PREDX-DOA1384N
FDA UDI
Class IIActive
Reveal ASC-RCUP-964N
FDA UDI
Class IIActive
Discover Plus DISPDUD9134NSO
FDA UDI
Class IIActive
Discover ASC-SAL-17104
FDA UDI
Class IIActive
Reveal ASCRMCUP2554SP
FDA UDI
Class IIActive
OneScreen ASC-DOA-544
FDA UDI
Class IIActive
Discover Plus DISP-DOA-865N
FDA UDI
UActive
Discover DIS-CUP18124MT
FDA UDI
Class IIActive
Precision DX PREDX-DOA4124N
FDA UDI
Class IIActive
Reveal ASC-RMCUP-2454
FDA UDI
Class IIActive
Reveal ASC-RCUP-6134N
FDA UDI
Class IIActive
Precision DX PREDX-CUP-274N
FDA UDI
Class IIActive
Precision Plus PREPLCUP6134
FDA UDI
Class IIActive
Discover Plus DISP-DOA-274N
FDA UDI
Class IIActive
Discover Plus DISPCUP7124DRK
FDA UDI
UActive
Precision DX PREDX-OFM-264N
FDA UDI
Class IIActive
Discover Plus DISP-CUP6124IB
FDA UDI
Class IIActive
Precision DX PREDX-CUP2144N
FDA UDI
Class IIActive
Discover Plus DISPDUD5104WVU
FDA UDI
Class IIActive
Reveal ASC-RCUP-264NC
FDA UDI
UActive
Discover Plus DISP-DUD-154N
FDA UDI
Class IIActive
Reveal ASCRMCUP2464MC
FDA UDI
Class IIActive
Discover DIS-DOA-154
FDA UDI
Class IIActive
Discover ASC-OSAL-564
FDA UDI
Class IIActive
Reveal ASCRMDUD2104US
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.