Identity
- Trade Name
- ExoToe FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
- Device Name
- ExoToe Crimping Forceps FDA UDI
- Model / Reference
- FCP001 FDA UDI
- Description
- ExoToe Crimping Forceps FDA UDI
Identifiers
- Catalog Number
- FCP001 FDA UDI
- Primary DI / UDI-DI
- B605FCP001 FDA UDI
- 510(k) Number
- K172205 FDA UDI
- FDA Product Code
- JDR FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, scissors-like, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 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
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical soft-tissue manipulation forceps, scissors-like, reusable
ExoToe by Exotoe, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Surgical soft-tissue manipulation forceps, scissors-like, reusable.
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- AESCULAP — AESCULAP, INC. · Class I
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- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
Cleared under the same submission
K172205 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Exotoe, LLC
Sources (1)
- FDA UDI fa1f71a1-305d-4b53-9b8f-cb5cd735dc56 35 fields · synced Jun 6, 2026