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Data / Medical devices / United States / Bleckmann USA LLC

Bleckmann USA LLC: FDA-registered device maker in Columbus, OH, United States, 1 510(k) clearance

Bleckmann USA LLC is registered with the FDA (registration 3022426824) in Columbus, OH, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 18, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3022426824
Address
2626 Port Rd, Columbus, OH, United States, 43217
Owner or operator
Logistics Investmen 1 BV (10086306)
Roles
Repackager or relabeler
First device listed
October 28, 2022
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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 18, 2022K210823LYMA LaserOHSSubstantially EquivalentLyma Life , Ltd.accessdata.fda.gov

Compare with other makers

Updated March 18, 2022. 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.