FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
LacertaMatrix
K Number: K260218
·
Decision Feb 19, 2026
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
1
Review Days
27
Basic Information
- Device Name
- LacertaMatrix
- K Number
- K260218
- Device Class
- FDA unclassified
- Clearance Type
- Special
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Lacerta Life Sciences
- Date Received
- January 23, 2026
- Decision Date
- February 19, 2026
- Product Code
- KGN
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| KGN | Wound Dressing With Animal-Derived Material(S) | FDA unclassified | Unknown |
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