ASPEN SURGICAL

FDA Regulatory Profile

ASPEN SURGICAL appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2221-2024, Class II) was initiated on June 3, 2024.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2221-2024Class IIEndoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, June 3, 2024