Phoenix Medical Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 11
What Phoenix Medical Technology, Inc. makes
Phoenix Medical Technology, Inc. manufactures single-use patient examination gloves in latex, nitrile, and vinyl formulations, including powder-free and low-powder variants, as well as color-coded options. Their portfolio also includes modified latex examination gloves and disposable patient examination drapes treated with antimicrobial agents. The company produces both standard and modified versions of latex gloves for medical use.
The company’s products are regulated under FDA’s Class I and Class II device classifications, with relevant submissions listed in the FDA’s 510(k) registry. These items are intended for use in clinical examinations and procedures, adhering to U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Phoenix Medical Technology, Inc. have in the registry?
The registry currently lists 11 devices for Phoenix Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phoenix Medical Technology, Inc.'s devices?
Among its 11 most recently registered devices, Phoenix Medical Technology, Inc. has devices listed in FDA 510(k) (11 devices).
What risk classes do Phoenix Medical Technology, Inc.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Phoenix Medical Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Phoenix Medical Technology, Inc. in the registry?
The most recently registered devices listed for Phoenix Medical Technology, Inc. include DOBE (MODIFIED), PATIENT EXAMINATION GLOVES, LOW POWDER SINGLE USE LATEX EXAM GLOVES and PATIENT EXAMINATION GLOVE.