FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Aurolab
Aurolab
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K221759
Cornisol
October 5, 2022
K140039
POLYCRYL
September 15, 2014
K024090
NYLON SUTURE
February 28, 2003
K024091
SILK SUTURES
February 28, 2003