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/ Gelesis, Inc.
Gelesis, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K230133
Plenity
January 19, 2024
DEN180060
Plenity
April 12, 2019