Lansinoh Laboratories Inc

FDA Regulatory Profile

Lansinoh Laboratories Inc appears in FDA public data with 1 recall, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0784-2013, Class II) was initiated on August 14, 2012. Its most recent 510(k) clearance was granted on June 30, 2023.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0784-2013Class IITHERA PEARL 3-in-1 BREAST THERAPY, 2 hot and cold packs in plastic box. The Thera Pearl 3-in-1 August 14, 2012

Recent 510(k) Clearances

K-NumberDeviceDate
K230469Compact Wearable PumpJune 30, 2023
K222726Smartpump 3.0 Double Electric Breast PumpDecember 23, 2022