PAJUNK GmbH Medizintechnologie is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
PAJUNK GmbH Medizintechnologie - FDA 510(k) Cleared Devices
Recent clearances: SonoMSK, SonoPlex STIM, SPROTTE® STANDARD (LUER/ NRFit®) Lumbar Puncture
44
Total
44
Cleared
0
Denied
PAJUNK GmbH Medizintechnologie has 44 FDA 510(k) cleared medical devices. Based in Geisingen, DE.
Latest FDA clearance: Jul 2025. Active since 2006. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by PAJUNK GmbH Medizintechnologie Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - PAJUNK GmbH Medizintechnologie
44 devices
Cleared
Jul 01, 2025
SonoMSK
Anesthesiology
214d
Cleared
Jun 27, 2025
SonoPlex STIM
Anesthesiology
210d
Cleared
Jun 25, 2025
SPROTTE® STANDARD (LUER/ NRFit®) Lumbar Puncture
Anesthesiology
103d
Cleared
Mar 24, 2025
SonoTAP and SonoTAP II
Anesthesiology
130d
Cleared
Nov 22, 2024
SPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology
Anesthesiology
142d
Cleared
Sep 11, 2024
SonoBlock
Anesthesiology
70d
Cleared
Nov 24, 2023
Stim2Go
Physical Medicine
255d
Cleared
Feb 22, 2023
Disposable Pre-calibrated Brain Biopsy Needle 2.0
Neurology
28d
Cleared
Aug 17, 2022
Disposable Brain Biopsy Needle 2.0
Neurology
142d
Cleared
Dec 29, 2020
E-Cath STIM acc. Tsui
Anesthesiology
104d
Cleared
Jun 17, 2019
Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-6
Anesthesiology
94d
Cleared
May 16, 2019
VPC
Anesthesiology
91d
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