FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001)
K Number: K260255
·
Decision Mar 27, 2026
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
1
Review Days
58
Basic Information
- Device Name
- AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001)
- K Number
- K260255
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4400
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Aventix Medical, Inc.
- Date Received
- January 28, 2026
- Decision Date
- March 27, 2026
- Product Code
- GEI
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- EN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | FDA class 2 | General, Plastic Surgery |
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