Harps Europe Manufacturing GmbH

FDA Regulatory Profile

Harps Europe Manufacturing GmbH appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 19, 2025.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K250313Sterile Powder Free Synthetic Rubber Surgeon’s Gloves, Green Color, Tested For Use With ChemotherapyAugust 19, 2025