Hurri-Freeze 115mL Medium Stream
by Beutlich Pharmaceuticals, LLC
Hurri-Freeze 115mL Medium Stream is a cold/cool therapy spray (FDA unclassified; FDA product code MLY, Vapocoolant Device) made by Beutlich Pharmaceuticals, LLC, cleared under FDA 510(k) K232674 on 12 Feb 2024 and listed in FDA GUDID since 15 Dec 2025 (UDI-DI 10723797807443), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10723797807443 | Date15 Dec 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK232674 | Date12 Feb 2024 | StatusActive |
Official records
- AccessGUDID record 10723797807443
- FDA 510(k) database K232674
Across registries
- FDA 510(k) K232674 decided 12 Feb 2024 Active
- FDA GUDID UDI-DI 10723797807443 listed 15 Dec 2025 Listed
Timeline
- Cleared FDA 510(k) K232674
- Listed FDA GUDID 10723797807443
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Hurri-Freeze
- Generic name
- Cold/cool therapy spray
- Model / reference
- 115mL Medium Stream
- Primary DI / UDI-DI
- 10723797807443
- 510(k) Number
- FDA product code
- MLY
- GMDN term
- Cold/cool therapy spray
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
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