Brius Technologies, Inc.
Brius Technologies, Inc. holds FDA 510(k) medical device clearances, cleared in 2021, with 3 FDA device recalls on record.
Top product codes for Brius Technologies, Inc.
FDA recalls by Brius Technologies, Inc.
- Z-0888-2022 — Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL
- Z-0889-2022 — Brius Patient Specific Brackets (components in a set of custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL
- Z-0890-2022 — Customized Brius Appliances (custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 52345400UL
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Brius Technologies, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.