Tempo Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Tempo Technology, Inc. makes
Tempo Technology, Inc. manufactures disposable cold therapy packs for acute injury management and portable X-ray systems for dental and medical diagnostics, including intraoral and general-purpose imaging units.
The company’s products are regulated under FDA’s Class I and Class II categories, with relevant devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Tempra Cold Pack, Reorder No. TC150 Ref K963220
Regimes: 510(k) Registry: 510(k)Trimode Sp Dental Intra Oral X-Ray Ref K896963
Regimes: 510(k) Registry: 510(k)Model 90P Portable Medical Diagnostic X-Ray Ref K934700
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tempo Technology, Inc. have in the registry?
The registry currently lists 3 devices for Tempo Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tempo Technology, Inc.'s devices?
Among its 3 most recently registered devices, Tempo Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Tempo Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Tempo Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tempo Technology, Inc. in the registry?
The most recently registered devices listed for Tempo Technology, Inc. include TEMPRA COLD PACK, REORDER NO. TC150, TRIMODE SP DENTAL INTRA ORAL X-RAY and MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY.