Theratechnologies, Inc.
CanadaFDA applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Theratechnologies, Inc. makes
Theratechnologies, Inc. manufactures STETHOS, a diagnostic device for auscultation, and ERADIC-ALL, a medical instrument designed for targeted antimicrobial treatment in specific clinical applications.
The company’s products are classified under Class I and Class II devices in the U.S. and are listed in the FDA 510(k) registry. The manufacturer is based in the United States.
Catalogue
Stethos Ref K963621
Regimes: 510(k) Registry: 510(k)Eradic-All Ref K981171
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Theratechnologies Inc. Montreal Quebec · CA FEI 3011453824
Frequently asked questions
How many devices does Theratechnologies, Inc. have in the registry?
The registry currently lists 2 devices for Theratechnologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theratechnologies, Inc.'s devices?
Among its 2 most recently registered devices, Theratechnologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Theratechnologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Theratechnologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Theratechnologies, Inc. in the registry?
The most recently registered devices listed for Theratechnologies, Inc. include STETHOS and ERADIC-ALL.
Which FDA establishments are linked to Theratechnologies, Inc.?
1 FDA establishment is linked to Theratechnologies, Inc. in the registry; they are listed on the company page.