Identity
- Trade Name
- Checkpoint Nerve Repair Kit FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
- Device Name
- The CHECKPOINT NERVE REPAIR KIT is a convenience kit of two (2) NeuroShield chitosan membranes (30mm x 20mm) and one (1) Checkpoint Edge Nerve Cutting Kit. FDA UDI
- Model / Reference
- NS3020K2 FDA UDI
- Description
- The CHECKPOINT NERVE REPAIR KIT is a convenience kit of two (2) NeuroShield chitosan membranes (30mm x 20mm) and one (1) Checkpoint Edge Nerve Cutting Kit. FDA UDI
Identifiers
- Catalog Number
- NS3020K2 FDA UDI
- Primary DI / UDI-DI
- B130NS3020K23 FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, single-use FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical soft-tissue manipulation forceps, tweezers-like, single-useNerve guide, animal-derived
Checkpoint Nerve Repair Kit by Checkpoint Surgical, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nerve guide, animal-derived.
- AxoGuard — COOK BIOTECH INCORPORATED · Class II
- NeuraGen® — Integra Lifesciences Corp. · Class II
- AxoGuard — COOK BIOTECH INCORPORATED · Class II
- NeuroFlex — COLLAGEN MATRIX, INC. · Class II
- NeuroMatrix — COLLAGEN MATRIX, INC. · Class II
- AxoGuard — COOK BIOTECH INCORPORATED · Class II
- AxoGuard Nerve Cap — AxoGen Corporation · Class II
- ConformaWrap — Biocircuit Technologies, Inc. · Class II
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 | N/A | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Checkpoint Surgical, Inc.
Sources (1)
- FDA UDI 345774fa-d2f6-44bd-9b56-8e1a512c8277 35 fields · synced Jun 8, 2026