PAJUNK GmbH Medizintechnologie FDA Approvals

0 new drug approvals and 9 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product	What it is	Route	Decided
SonoMSK510(k)Jul 1, 2025Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Jul 1, 2025
SonoPlex STIM; SonoPlex II510(k)Jun 27, 2025Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Jun 27, 2025
SPROTTE® STANDARD (LUER/ NRFit®) Lumbar Puncture510(k)Jun 25, 2025Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Jun 25, 2025
SonoTAP and SonoTAP II510(k)Mar 24, 2025Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Mar 24, 2025
SPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology510(k)Nov 22, 2024Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Nov 22, 2024
SonoBlock; SonoBlock II510(k)Sep 11, 2024Anesthesiology	Anesthesiology	510(k)Substantially Equivalent (Traditional)	Sep 11, 2024
Stim2Go510(k)Nov 24, 2023Physical Medicine	Physical Medicine	510(k)Substantially Equivalent (Traditional)	Nov 24, 2023
Disposable Pre-calibrated Brain Biopsy Needle 2.0510(k)Feb 22, 2023Neurology	Neurology	510(k)Substantially Equivalent (Special)	Feb 22, 2023
Disposable Brain Biopsy Needle 2.0510(k)Aug 17, 2022Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Aug 17, 2022