Midas Intl. Development Corp.
PH Last updated 22 Oct 2026
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- Devices
- 1
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Latex Examination Gloves Ref K893296
What Midas Intl. Development Corp. makes
Midas Intl. Development Corp. manufactures latex examination gloves, designed for medical and clinical use to ensure sterile protection during examinations and procedures.
These products fall under FDA Class I devices and are listed via the 510(k) pathway. The company is based in the United States.
Frequently asked questions
What types of medical devices does Midas Intl. Development Corp. manufacture?
Midas Intl. Development Corp. specializes in latex examination gloves, which are intended for medical and clinical use. These gloves are designed to provide sterile protection during examinations and procedures, ensuring hygiene and safety for both patients and healthcare providers.
Where is Midas Intl. Development Corp. based?
Midas Intl. Development Corp. is headquartered in the United States. This location allows the company to operate within the regulatory framework of the FDA, which governs the manufacturing and distribution of medical devices in the country.
Which regulatory registries or databases list Midas Intl. Development Corp.’s devices?
Midas Intl. Development Corp.’s latex examination gloves are listed in the FDA’s 510(k) registry. The 510(k) pathway is used for Class I devices that are not low-risk but require demonstration of substantial equivalence to a predicate device already on the market.
How are Midas Intl. Development Corp.’s devices classified by regulatory authorities?
Midas Intl. Development Corp.’s latex examination gloves are classified as FDA Class I devices. This classification applies because the gloves are considered low-risk, non-invasive, and generally do not require active controls or complex mechanisms, though they still must meet performance and safety standards.
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