Medi-Tech Intl. Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Medi-Tech Intl. Corp. makes
Medi-Tech Intl. Corp. manufactures sterile aloe vera-based wound care products, including the Diamond Aloe Vera formulation, as well as granulated gel dressings like Spand-Gel. The company also produces protective restraints designed for patient safety applications.
The company’s portfolio includes devices classified as Class I and Unclassified (U), with some products subject to 510(k) clearance via the FDA’s regulatory pathway. These devices are listed under the U.S. Food and Drug Administration’s 510(k) premarket notification process.
Catalogue
Diamond Aloe Vera, Sterile Ref K002666
Regimes: 510(k) Registry: 510(k)Protective Restraint Ref K110377
Regimes: 510(k) Registry: 510(k)Spand-Gel Granulated Gel Ref K864124
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi-Tech Intl. Corp. have in the registry?
The registry currently lists 3 devices for Medi-Tech Intl. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Tech Intl. Corp.'s devices?
Among its 3 most recently registered devices, Medi-Tech Intl. Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Medi-Tech Intl. Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medi-Tech Intl. Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Tech Intl. Corp. in the registry?
The most recently registered devices listed for Medi-Tech Intl. Corp. include DIAMOND ALOE VERA, STERILE, PROTECTIVE RESTRAINT and SPAND-GEL GRANULATED GEL.