Identity
- Trade Name
- Exodus Revision FDA UDI
- Generic Name
- Orthopaedic osteotome blade, single-use FDA UDI
- Model / Reference
- 00-510-400-00 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850019455717 FDA UDI
- FDA Product Code
- KDD FDA UDI
- GMDN Term
- Orthopaedic osteotome blade, 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic osteotome blade, single-use
Exodus Revision by Tightline Development — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic osteotome blade, single-use.
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- RP Medical — Rp Medical, Inc. · Class I
- IMEDICOM HIGH SPEED BLADE — IMEDICOM CO., LTD. · 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 |
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Manufacturer
- Manufacturer
- Tightline Development
Sources (1)
- FDA UDI a33c05a9-8f49-40d2-9fd0-7de35a5223d2 32 fields · synced May 30, 2026