Makintech Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Makintech Corp. makes
Makintech Corp. manufactures latex surgical gloves for non-sterile use and latex examination gloves, designed for medical and clinical applications.
These products are classified as Class I devices under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Latex Surgical Glove (Non Sterile) Ref K883556
Regimes: 510(k) Registry: 510(k)Latex Examination Gloves Ref K893176
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Makintech Corp. have in the registry?
The registry currently lists 2 devices for Makintech Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Makintech Corp.'s devices?
Among its 2 most recently registered devices, Makintech Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Makintech Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Makintech Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Makintech Corp. in the registry?
The most recently registered devices listed for Makintech Corp. include LATEX SURGICAL GLOVE (NON STERILE) and LATEX EXAMINATION GLOVES.