Faxitron Bioptics, LLC

FDA Regulatory Profile

Faxitron Bioptics, LLC appears in FDA public data with 0 recalls, 5 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 14, 2019.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K183142PathVisionXLMarch 14, 2019
K173309Faxitron VisionCTMay 9, 2018
K170786Faxitron Bioptics Speciemen Radiography SystemJuly 18, 2017
K153583BioVision PlusApril 1, 2016
K122428FAXITRON SPECIEN RADIOGRAPHY SYSTEMSeptember 25, 2012