Archtek, Inc.
United StatesFDA applicant, unverified FDA FEI 3000203342
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Archtek, Inc. makes
Archtek, Inc. makes devices such as the GRIND GUARD, which is a type of dental device.
The company's portfolio is regulated and listed in the fda_510k registry, with devices classified as Class U, and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Grind Guard Ref K073446
Regimes: 510(k) Registry: 510(k)Grind Guard Ref K090472
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3000203342
- Address
- 11405 N. Pennsylvania St., Carmel, IN, 46032
Frequently asked questions
How many devices does Archtek, Inc. have in the registry?
The registry currently lists 2 devices for Archtek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Archtek, Inc.'s devices?
Among its 2 most recently registered devices, Archtek, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Archtek, Inc. in the registry?
The most recently registered devices listed for Archtek, Inc. include GRIND GUARD.