Mastri Lieno, PT
ID Last updated 22 Oct 2026
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- Devices
- 1
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Patient Examination Glove Ref K902770
What Mastri Lieno, PT makes
Mastri Lieno, PT manufactures patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
The company’s products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Frequently asked questions
What types of medical devices does Mastri Lieno, PT manufacture?
Mastri Lieno, PT specializes in patient examination gloves, which are intended for single-use during medical procedures. These gloves are designed to help maintain hygiene and minimize infection risks during clinical examinations.
Where is Mastri Lieno, PT based, and does it operate internationally?
Mastri Lieno, PT is based in the United States. While the company’s headquarters and primary operations are located there, the question of international operations would depend on specific regulatory filings or market presence, which are not provided in the available data.
How are Mastri Lieno, PT’s devices classified under FDA regulations?
Mastri Lieno, PT’s patient examination gloves fall under Class I classification according to FDA regulations. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, such as disposable gloves used for routine hygiene purposes.
Which regulatory registries or databases list Mastri Lieno, PT’s devices?
Mastri Lieno, PT’s devices are listed in the FDA’s 510(k) registry, which documents medical devices that have undergone the 510(k) premarket notification process. This pathway is used for devices deemed substantially equivalent to legally marketed predicates, ensuring compliance with FDA requirements.
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