FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Fem Suite, LLC
Fem Suite, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K093218
FEMEYE TWO
May 18, 2010
K062563
FEMTEN CERVICAL TENACULUM
May 18, 2007