Alcon Grieshaber AG

FDA Regulatory Profile

Alcon Grieshaber AG appears in FDA public data with 1 recall, 0 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1506-2013, Class II) was initiated on April 17, 2013.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1506-2013Class IIThe Constellation Vision System Pneumatic Handpiece. Indicated for both anterior and posterior seApril 17, 2013