Al Nyman & Son, Inc.
Country not established
- Devices
- 1
What Al Nyman & Son, Inc. makes
Al Nyman & Son, Inc. manufactures the ALSITE MAGNIVISION, a device designed for magnifying and illuminating surgical fields to enhance precision during procedures.
The ALSITE MAGNIVISION is classified under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Alsite Magnivision Ref K772228
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Al Nyman & Son, Inc. have in the registry?
The registry currently lists 1 device for Al Nyman & Son, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Al Nyman & Son, Inc.'s devices?
Among its 1 most recently registered device, Al Nyman & Son, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Al Nyman & Son, Inc. in the registry?
The most recently registered devices listed for Al Nyman & Son, Inc. include ALSITE MAGNIVISION.