Identity
- Trade Name
- AYON Ultrasound Assisted Liposuction Cable FDA UDI
- Generic Name
- Liposuction system FDA UDI
- Model / Reference
- AYON-UAL-0002 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00607151050566 FDA UDI
- 510(k) Number
- K244050 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
Yes
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Liposuction system
AYON Ultrasound Assisted Liposuction Cable by Apyx Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Liposuction system.
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- ORIGINS — Solta Medical, Inc. · Class II
- Alma LipoFlow System 50Hz — ALMA LASERS LTD. · Class II
- AirSculpt Handpiece — Millennium Medical Technologies, Inc. · Class II
- SUMMIT MEDICAL — Summit Medical, LLC · Class II
Cleared under the same submission
K244050 also covers:
- AYON Base Tower — Apyx Medical Corporation
- AYON Base Tower — Apyx Medical Corporation
- AYON Body Contouring System — Apyx Medical Corporation
- AYON Console — Apyx Medical Corporation
- AYON Infiltration Handle — Apyx Medical Corporation
- AYON Infiltration Handle on/off — Apyx Medical Corporation
- AYON Skin Port Corckscrew — Apyx Medical Corporation
- AYON Skin Port Large 5mm — Apyx Medical Corporation
- AYON Skin Port Small 3mm — Apyx Medical Corporation
- AYON Skin Port Tool — Apyx Medical Corporation
- AYON Suction Assisted Liposuction Handle — Apyx Medical Corporation
- AYON Ultrasound Assisted Liposuction Handpiece — Apyx Medical Corporation
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Apyx Medical Corporation
Sources (1)
- FDA UDI 7b3c5e5a-affc-4f2b-a0e2-0c501d7c86ea 33 fields · synced Jun 9, 2026