Home › Guangzhou Decheng Biotechnology Co., LTD › UScreen

UScreen

Guangzhou Decheng Biotechnology Co., LTD · Model USSCUPA-12CLIA · UDI-DI 00850054867926

NGG NFT PTH NGL NFV NFY PTG NGM QBF DJG QAW NFW

510(k) clearances

Adverse events

Recalls

Facilities

Description

UScreen™ RAPID DRUG TEST CUP, 12-Panel, 25T/Box

Recalls

Date	Firm	Reason
2017-09-30	Ameditech Inc	Product was released to market without the adulteration strip included in the product.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.