Data / Medical devices / United States / Hinlab Inc.

Hinlab Inc.: FDA-registered device maker in Lewes, DE, United States, 1 510(k) clearance

Hinlab Inc. is registered with the FDA (registration 3044675072) in Lewes, DE, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 21, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3044675072

Address

412 Canary Ct, Lewes, DE, United States, 19958

Owner or operator

hinlab Inc. (10095681)

Roles

Complaint file establishment, Specification developer

First device listed

April 14, 2026

Registered through

2026

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

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Updated December 21, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.