Whitmore Ent., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Whitmore Ent., Inc. makes
Whitmore Ent., Inc. manufactures the Whitmore Ankle X-Ray Extension, a device designed for immobilizing and positioning the ankle during radiographic imaging, and the Whitmore Vacuum-Lock Spinal Frame (VLSF-100), a spinal immobilization frame used for stabilizing the cervical spine and torso under vacuum suction.
The company’s products are regulated under FDA Class I and Class II classifications, with the Ankle X-Ray Extension and Vacuum-Lock Spinal Frame listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Whitmore Ankle X-Ray Extension (Axe) Ref K933778
Regimes: 510(k) Registry: 510(k)Whitmore Vacuum-Lock Spinal Frame (Vlsf-100) Ref K931037
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Whitmore Ent., Inc. have in the registry?
The registry currently lists 2 devices for Whitmore Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whitmore Ent., Inc.'s devices?
Among its 2 most recently registered devices, Whitmore Ent., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Whitmore Ent., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Whitmore Ent., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Whitmore Ent., Inc. in the registry?
The most recently registered devices listed for Whitmore Ent., Inc. include WHITMORE ANKLE X-RAY EXTENSION (AXE) and WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100).