Nvision Biomedical Technologies, Inc
United Statesfrom the FDA registration address FDA establishment FEI 3011301313
- Devices
- 1,841
- Registrations
- FDA
- FDA recalls
- 0
What Nvision Biomedical Technologies, Inc makes
NVISION Biomedical Technologies, Inc makes orthopaedic and spinal implants and instruments, including internal fixation system implantation kits, bone screws, spinal interbody fusion cages, and spinal fixation plates. Their products also include surgical instruments such as reusable tamps and implant racks.
The company's portfolio is regulated under Class I and Class II devices and is listed in the FDA UDI registry. The company is based in the US.
Catalogue
Search and filter all 1,841 devicesShowing 1-50 of 1,841
Company details
- FDA FEI number
- 3011301313
- Address
- 12449 Silicon Dr, San Antonio, TX, 78249
Frequently asked questions
How many devices does NVISION BIOMEDICAL TECHNOLOGIES, INC have in the registry?
The registry currently lists 1841 devices for NVISION BIOMEDICAL TECHNOLOGIES, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list NVISION BIOMEDICAL TECHNOLOGIES, INC's devices?
Among its 50 most recently registered devices, NVISION BIOMEDICAL TECHNOLOGIES, INC has devices listed in FDA 510(k) (1 device) and FDA GUDID (49 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do NVISION BIOMEDICAL TECHNOLOGIES, INC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for NVISION BIOMEDICAL TECHNOLOGIES, INC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from NVISION BIOMEDICAL TECHNOLOGIES, INC in the registry?
The most recently registered devices listed for NVISION BIOMEDICAL TECHNOLOGIES, INC include Ntegrate Threaded Nail System, Healix CSRW-1000T-310, Healix CSRW-1000T-320 and Healix CSRW-1000T-311.