Arnold Tuber Industries
United Statesfrom the FDA registration address FDA establishment FEI 3003988575
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Arnold Tuber Industries makes
Arnold Tuber Industries manufactures aspirating syringes and non-aspirating syringes.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Aspirating Syringe, Non-Aspirating Syringe Ref K092943
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003988575
- Address
- 10 Centre Dr, Orchard Park, NY, 14127
Frequently asked questions
How many devices does ARNOLD TUBER INDUSTRIES have in the registry?
The registry currently lists 1 device for ARNOLD TUBER INDUSTRIES. Devices recorded under merged duplicate company entries are counted once.
Which registries list ARNOLD TUBER INDUSTRIES's devices?
Among its 1 most recently registered device, ARNOLD TUBER INDUSTRIES has devices listed in FDA 510(k) (1 device).
What risk classes do ARNOLD TUBER INDUSTRIES's devices fall under?
Among its 1 most recently registered device, the classes recorded for ARNOLD TUBER INDUSTRIES's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ARNOLD TUBER INDUSTRIES in the registry?
The most recently registered devices listed for ARNOLD TUBER INDUSTRIES include ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE.