Galaxy Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Galaxy Intl., Inc. makes
Galaxy Intl., Inc. manufactures sterile and non-sterile patient examination gloves, as well as surgical gloves.
The company is based in the United States, and its devices are classified as Class I and listed within the FDA 510(k) regulatory registry.
Catalogue
Sterile Patient Examination Gloves Ref K891329
Regimes: 510(k) Registry: 510(k)Grand Guard Surgical Gloves Ref K892061
Regimes: 510(k) Registry: 510(k)Non-Sterile Patient Examination Gloves Ref K891330
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Galaxy Intl., Inc. have in the registry?
The registry currently lists 3 devices for Galaxy Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Galaxy Intl., Inc.'s devices?
Among its 3 most recently registered devices, Galaxy Intl., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Galaxy Intl., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Galaxy Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Galaxy Intl., Inc. in the registry?
The most recently registered devices listed for Galaxy Intl., Inc. include STERILE PATIENT EXAMINATION GLOVES, GRAND GUARD SURGICAL GLOVES and NON-STERILE PATIENT EXAMINATION GLOVES.