PAJUNK GmbH Medizintechnologie - FDA 510(k) Cleared Devices
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) cleared devices by 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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