Identity
- Trade Name
- DEKA SMARTXIDE PRO FDA UDI
- Generic Name
- Dermatological carbon dioxide laser system FDA UDI
- Device Name
- The SmartXide PRO is a medical device indicated for incision, excision, ablation, vaporization and coagulation of body soft tissues incluing intraoral tissues, in medical specialties including aesthetic (dermatology and plastic surgery), otolaryngology (ENT), gynaecology, neurosurgery, dental and oral surgery and genitourinary surgery. The use with the scanning unit is indicated for ablative skin resurfacing. FDA UDI
- Model / Reference
- M079BI1 FDA UDI
- Description
- The SmartXide PRO is a medical device indicated for incision, excision, ablation, vaporization and coagulation of body soft tissues incluing intraoral tissues, in medical specialties including aesthetic (dermatology and plastic surgery), otolaryngology (ENT), gynaecology, neurosurgery, dental and oral surgery and genitourinary surgery. The use with the scanning unit is indicated for ablative skin resurfacing. FDA UDI
Identifiers
- Catalog Number
- M079R1 FDA UDI
- Primary DI / UDI-DI
- 08034108512709 FDA UDI
- 510(k) Number
- K240537 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Dermatological carbon dioxide laser system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dermatological carbon dioxide laser system
Deka Smartxide Pro by Deka M.e.l.a. Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Deka M.e.l.a. Srl
Sources (1)
- FDA UDI eb6066ef-34f5-48fd-9f69-739dc5d70b5f 36 fields · synced Jun 9, 2026