BioXtreme
Country not established FDA FEI 3016569182
- Devices
- 0
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What BioXtreme makes
BioXtreme manufactures the DeXtreme and PlaXtreme devices, which appear to be Class I medical products designed for specific clinical applications, though exact uses are not detailed. These products are likely intended for low-risk procedures or diagnostic purposes, such as wound care or minimally invasive treatments.
The company’s portfolio is regulated under EU medical device directives, with devices listed in the EUDAMED database. Both products fall under Class I classification, indicating minimal risk and regulatory oversight. The manufacturer is based in Israel.
Company details
- FDA FEI number
- 3016569182
- Address
- 7 Imber Street, Petach Tikva Central