Identity
- Trade Name
- AirSculpt Console FDA UDI
- Generic Name
- Liposuction system FDA UDI
- Model / Reference
- AIRS-1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850000712201 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Liposuction system
AirSculpt Console by Millennium Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Liposuction system.
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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 f6b0cefb-80b0-4ed6-90c6-1c6c8a61a493 33 fields · synced May 30, 2026