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Ormed GmbH

FDA Regulatory Profile

Ormed GmbH appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 29, 1997.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K964799ARTROTHERM CRYOTHERAPY AND THERNOTHERAPYAugust 29, 1997
K964354ARTOCOOL-S WATER CIRCULATING COLD PACKAugust 29, 1997

FDA data resources