Altor Safety
United Statesfrom the FDA registration address FDA establishment FEI 3016966810
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
What Altor Safety makes
Altor Safety manufactures single-use, non-antimicrobial surgical and medical face masks, including 3-ply and 4-ply variants designed for clinical and procedural use.
The company’s products are regulated as Class II devices in the US, with models listed under FDA 510(k) and UDI requirements. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Altor Safety 3-Ply Surgical Mask (Model:62222) Ref K211249
Regimes: 510(k) Registry: 510(k)Altor Safety 4-Ply Surgical Mask (Model:62232) Ref K211762
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016966810
- Address
- 711 Executive Blvd, Valley Cottage, NY, 10989
Frequently asked questions
How many devices does ALTOR SAFETY have in the registry?
The registry currently lists 8 devices for ALTOR SAFETY. Devices recorded under merged duplicate company entries are counted once.
Which registries list ALTOR SAFETY's devices?
Among its 8 most recently registered devices, ALTOR SAFETY has devices listed in FDA 510(k) (2 devices) and FDA GUDID (6 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ALTOR SAFETY's devices fall under?
Among its 8 most recently registered devices, the classes recorded for ALTOR SAFETY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ALTOR SAFETY in the registry?
The most recently registered devices listed for ALTOR SAFETY include Altor Safety 62232, Altor Safety 62222, Altor Safety 3-Ply Surgical Mask (Model:62222) and Altor Safety 4-Ply Surgical Mask (Model:62232).