Identity
- Trade Name
- Fox Curettes FDA UDI
- Generic Name
- Dermal curette, single-use FDA UDI
- Device Name
- A sterile, hand-held manual surgical instrument designed exclusively for the precise scraping and/or excising of skin/dermal tissue (e.g., for treatment of superficial warts or wounds). It is available in a variety of shapes/sizes and has an appropriately-shaped distal end (e.g., ring-like). This is a single-use device. FDA UDI
- Model / Reference
- 11-020-03 FDA UDI
- Description
- A sterile, hand-held manual surgical instrument designed exclusively for the precise scraping and/or excising of skin/dermal tissue (e.g., for treatment of superficial warts or wounds). It is available in a variety of shapes/sizes and has an appropriately-shaped distal end (e.g., ring-like). This is a single-use device. FDA UDI
Identifiers
- Catalog Number
- 11-020-03 FDA UDI
- Primary DI / UDI-DI
- G25011020030 FDA UDI
- FDA Product Code
- HTF FDA UDI
- GMDN Term
- Dermal curette, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 14 Centimeter FDA UDI
Category: Dermal curette, single-use
Fox Curettes by N S Surgical Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dermal curette, single-use.
- American Medicals — AMERICAN MEDICALS · Class I
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
- Hayden Medical — Hayden Medical Inc · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- Sklar® — Sklar Corporation · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- BR Surgical, LLC — BR SURGICAL LLC · 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
- N S Surgical Company
Sources (1)
- FDA UDI 21bd8671-cd9b-4fb0-9bbf-c808a4165047 35 fields · synced May 30, 2026