Registered with FDA
Altitude Technologies, Inc DBA Chinook Medical Gear
Tulsa, OK, United States. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 0
- 510(k) clearances
- 0as applicant
- Markets registered in
- 24 registrations outside the US
- Establishments
- 1United States
Registered in 2 markets
Where regulators' registries name Altitude Technologies, Inc DBA Chinook Medical Gear as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Lister | Altitude Technologies, Inc DBA Chinook Medical Gear | 1 device types | — | Below |
| Israel | AMAR | Manufacturer | Chinook Medical Gear Inc | 4 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Altitude Technologies, Inc DBA Chinook Medical Gear currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| General Purpose Dental TrayOFX · Class 1 | — | Lister | — | 2014 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| CHINOOK MEDICAL GEAR, INC.FDA reg. 3004468406 | Tulsa, OK, United States | Repacker / relabeler |
Other names on FDA records
Chinook Medical Gear Inc
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10030316). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.