Brius Technologies Inc. FDA Recalls

3 recalls on file across devices, 0 of them Class I and 0 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Brius Patient Specific Brackets (components in a set of custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile,Class IIFeb 7, 2022Pontics, brackets, and customized orthodontic appliances wer	Pontics, brackets, and customized orthodontic appliances were sold and distributed prior to completing the sta	Class IIDevices	Feb 7, 2022
Brius Pontics (components in a set of custom metal orthodontic devices);BRIUS , RX Only, Non-Sterile, Custom Made DeviceClass IIFeb 7, 2022Pontics, brackets, and customized orthodontic appliances wer	Pontics, brackets, and customized orthodontic appliances were sold and distributed prior to completing the sta	Class IIDevices	Feb 7, 2022
Customized Brius Appliances (custom metal orthodontic devices); BRIUS , RX Only, Non-Sterile, Custom Made Device, ID: 5Class IIFeb 7, 2022Pontics, brackets, and customized orthodontic appliances wer	Pontics, brackets, and customized orthodontic appliances were sold and distributed prior to completing the sta	Class IIDevices	Feb 7, 2022