A. Henniss
Country not established
- Devices
- 3
What A. Henniss makes
A. Henniss manufactures surgical instruments for cranial and spinal procedures, including craniotomy blades and drill bits for bone resection, serrated fixation staples with spikes for secure tissue approximation, and spinal Adson-Beckman retractors for exposure during surgery.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These instruments are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Craniotome Blade Or Drill Bit Ref K902703
510(k) 510(k)- 510(k) 510(k)
Adson-Beckman Retractor, Spinal Ref K905445
510(k) 510(k)
Frequently asked questions
How many devices does A. Henniss have in the registry?
The registry currently lists 3 devices for A. Henniss. Devices recorded under merged duplicate company entries are counted once.
Which registries list A. Henniss's devices?
Among its 3 most recently registered devices, A. Henniss has devices listed in FDA 510(k) (3 devices).
What risk classes do A. Henniss's devices fall under?
Among its 3 most recently registered devices, the classes recorded for A. Henniss's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A. Henniss in the registry?
The most recently registered devices listed for A. Henniss include CRANIOTOME BLADE OR DRILL BIT, STAPLE, SERRATED, FIXATION W/SPIKES, VARIOUS SIZES and ADSON-BECKMAN RETRACTOR, SPINAL.