Mend Technologies, Inc.

FDA Regulatory Profile

Mend Technologies, 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 March 30, 1993.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K924094MEND APCMarch 30, 1993
K883867CERVICAL BIOPSY INSTRUMENTNovember 29, 1988
K884558IOP ADJUSTABLE STIRRUPNovember 17, 1988