Identity
- Trade Name
- AirSculpt System FDA UDI
- Generic Name
- Liposuction system FDA UDI
- Model / Reference
- AIRS-1-SYS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850000712331 FDA UDI
- 510(k) Number
- K241835 FDA UDI
- FDA Product Code
- QPB FDA UDI
- GMDN Term
- Liposuction system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Liposuction system
AirSculpt System by Millennium Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Liposuction system.
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- MicroAire® — MicroAire Surgical Instruments LLC · Class II
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- MicroAire® — MicroAire Surgical Instruments LLC · Class II
- ORIGINS — Solta Medical, Inc. · Class II
- Alma LipoFlow System 50Hz — ALMA LASERS LTD. · Class II
- SUMMIT MEDICAL — Summit Medical, LLC · Class II
Cleared under the same submission
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Millennium Medical Technologies, Inc.
Sources (1)
- FDA UDI 7da3544c-8519-4aeb-80ef-2d4a7b7efde0 33 fields · synced May 31, 2026