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Phoenix Bioengineering, Inc.

FDA Regulatory Profile

Phoenix Bioengineering, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 30, 1993.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K930125PHOENIX BONE SCREWS PBS-TYPE SERIESDecember 30, 1993
K913490PHOENIX BURR HOLE BUTTON, BURR 1January 13, 1992
K904434SEXTON CYSTOTOMY URINE PUMP (SCUP2)February 1, 1991

FDA data resources