Dinkler Surgical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Dinkler Surgical Devices, Inc. makes
Dinkler Surgical Devices, Inc. manufactures surgical instruments for cranial procedures, including the DINKLER SURGICAL SKULL CLAMP (Model 0308) and the LIMITED ARTIFACT SKULL PIN (Model 0107). These devices are designed for use in neurosurgical applications to secure or stabilize the skull during procedures.
The company’s portfolio consists of Class II medical devices, authorised through the FDA’s 510(k) clearance process. These devices are listed under the US regulatory framework and are intended for use in surgical settings requiring precise cranial fixation or minimal imaging interference.
Catalogue
Dinkler Surgical Skull Clamp, Model 0308 Ref K090695
Regimes: 510(k) Registry: 510(k)Limited Artifact Skull Pin, Model 0107 Ref K073163
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dinkler Surgical Devices, Inc. have in the registry?
The registry currently lists 2 devices for Dinkler Surgical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dinkler Surgical Devices, Inc.'s devices?
Among its 2 most recently registered devices, Dinkler Surgical Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dinkler Surgical Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dinkler Surgical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dinkler Surgical Devices, Inc. in the registry?
The most recently registered devices listed for Dinkler Surgical Devices, Inc. include DINKLER SURGICAL SKULL CLAMP, MODEL 0308 and LIMITED ARTIFACT SKULL PIN, MODEL 0107.