Nortech Laboratories, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 2415591
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Nortech Laboratories, Inc. makes
Nortech Laboratories, Inc. makes the Irriclear Ear Irrigation Syringe, a device used for ear irrigation.
The Irriclear Ear Irrigation Syringe is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Irriclear Ear Irrigation Syringe Ref K903759
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2415591
- Address
- 125 Sherwood Ave, E Farmingdale, NY, 11735
Frequently asked questions
How many devices does Nortech Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Nortech Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nortech Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Nortech Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nortech Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nortech Laboratories, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nortech Laboratories, Inc. in the registry?
The most recently registered devices listed for Nortech Laboratories, Inc. include IRRICLEAR EAR IRRIGATION SYRINGE.