Pro-Med Instruments GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pro-Med Instruments GmbH - FDA 510(k) Cleared Devices
Recent clearances: DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00), DORO LUCENT Skull Clamp (1101.001), DORO QR3 Headrest System (Aluminum)
10
Total
10
Cleared
0
Denied
Pro-Med Instruments GmbH has 10 FDA 510(k) cleared neurology devices. Based in Roswell, US.
Latest FDA clearance: Jul 2024. Active since 2000.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pro Med Instruments GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Pro-Med Instruments GmbH
10 devices
Cleared
Jul 26, 2024
DORO Sterile Disposable Skull Pins Stainless Steel, Adult (36 pcs) (3006-00)
Neurology
28d
Cleared
Apr 24, 2024
DORO LUCENT Skull Clamp (1101.001)
Neurology
82d
Cleared
Mar 29, 2021
DORO QR3 Headrest System (Aluminum)
Neurology
119d
Cleared
Jun 02, 2020
DORO Sterile Disposable Skull Pins (Stainless Steel) , DORO Sterile...
Neurology
174d
Cleared
Feb 21, 2020
DORO LUCENT® iXI and iMRI Headrest System
Neurology
235d
Cleared
Oct 22, 2019
DORO QR3 XTom Headholder System
Neurology
90d
Cleared
May 21, 2007
DORO RADIOLUCENT HEADREST SYSTEM ( ALSO MRI-COMPATIBLE) AND COMPONENTS
Neurology
182d
Cleared
May 16, 2007
DORO NON-STICK BIPOLAR FORCEPS, MODEL 5001-XX TO 5012-XX, DORO BIPOLAR...
General & Plastic Surgery
37d
Cleared
Nov 20, 2003
DORO RADIOLUCENT HEADREST SYSTEM AND HORSESHOE HEADRESTS,AND NON-RADIOLUCENT...
Neurology
114d
Cleared
Aug 04, 2000
DORO HEADREST SYSTEM
Neurology
50d