Drg Intl., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Drg Intl., Inc. makes
Drg Intl., Inc. manufactures enzyme immunoassay kits for hormone detection, including salivary tests for testosterone, 17-alpha-hydroxyprogesterone, and cortisol, as well as ELISA-based testosterone assays for auric acid analysis.
These products are regulated under FDA 510(k) clearance as Class I and Class II medical devices, with listings in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Drg Slv Testosterone Elisa Test Ref K052649
510(k) 510(k)Drg Aurica Elisa Testosterone Kit Ref K000043
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does Drg Intl., Inc. have in the registry?
The registry currently lists 4 devices for Drg Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Drg Intl., Inc.'s devices?
Among its 4 most recently registered devices, Drg Intl., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Drg Intl., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Drg Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Drg Intl., Inc. in the registry?
The most recently registered devices listed for Drg Intl., Inc. include DRG SLV TESTOSTERONE ELISA TEST, DRG AURICA ELISA TESTOSTERONE KIT, ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY 17-A-HYDROXYPROGESTERONE and ENZYME IMMUNOASSAY FOR THE DETECTION OF SALIVARY CORTISOL.