Identity
- Trade Name
- Sklar® FDA UDI
- Generic Name
- Cartilage knife FDA UDI
- Device Name
- MASING CARTILAGE KNIFE 5 1/8" FDA UDI
- Model / Reference
- 41-1258 FDA UDI
- Description
- MASING CARTILAGE KNIFE 5 1/8" FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10649111230028 FDA UDI
- FDA Product Code
- KAS FDA UDI
- GMDN Term
- Cartilage knife FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Cartilage knife
Sklar® by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cartilage knife.
- Symmetry Harrison — SYMMETRY SURGICAL INC. · Class I
- Drive — Drive Devilbiss Healthcare · Class I
- V. Mueller — STERIS CORPORATION · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- Symmetry Surgical — SYMMETRY SURGICAL INC. · Class I
- Symmetry Rosen — SYMMETRY SURGICAL INC. · Class I
- Symmetry Ballenger — SYMMETRY SURGICAL INC. · Class I
- Symmetry Paparella — SYMMETRY SURGICAL INC. · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sklar Corporation
Sources (1)
- FDA UDI a7bd5ab3-3070-442c-96da-c70b50a9bd32 33 fields · synced May 30, 2026