Medical Device Manufacturer · US , Dayton , OH

Dinkler Surgical Devices, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

Dinkler Surgical Devices, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dayton, US.

Historical record: 2 cleared submissions from 2008 to 2009. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Dinkler Surgical Devices, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dinkler Surgical Devices, Inc.

2 devices
1-2 of 2
Cleared Apr 23, 2009
DINKLER SURGICAL SKULL CLAMP, MODEL 0308
K090695 · HBL
Neurology · 38d
Cleared Feb 28, 2008
LIMITED ARTIFACT SKULL PIN, MODEL 0107
K073163 · HBL
Neurology · 111d
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