FDA Data MCP
☰
Docs
Datasets
Pricing
Blog
Account
Statistics
Get API Key
Home
/
Companies
/ Timpel, Inc.
Timpel, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250464
Enlight 2100 (TPL-E2103-0)
September 10, 2025
K222897
Enlight 2100
March 7, 2023
K211135
Enlight 2100
January 6, 2022
DEN170072
Enlight 1810
December 20, 2018