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/ Tulavi Therapeutics
Tulavi Therapeutics
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252051
allay Nerve Cap (TL5515-1); allay Nerve Cap (TL5515-2); Delivery Tips (TL-7627)
September 29, 2025
DEN230061
allay Nerve Cap
July 16, 2024