P&A USA

FDA Regulatory Profile

P&A USA appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 9, 2025.

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243731HEXIM Implant; Samwon General AbutmentsJuly 9, 2025