Identity
- Trade Name
- SmartLOX Cervical Plate System FDA UDI
- Generic Name
- Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system FDA UDI
- Device Name
- Plate Bender FDA UDI
- Model / Reference
- CP50210 FDA UDI
- Description
- Plate Bender FDA UDI
Identifiers
- Primary DI / UDI-DI
- M739CP502100 FDA UDI
- 510(k) Number
- K141332 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system
SmartLOX Cervical Plate System by Captiva Spine — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system.
- Radial Pressure Pulse Therapy Device — Guangzhou Longest Medical Technology Co., Ltd. · Class I
- Radial Pressure Pulse Therapy Device — Guangzhou Longest Science & Technology Co., Ltd. · Class I
- Radial Pressure Pulse Therapy Device — Guangzhou Longest Medical Technology Co., Ltd. · Class I
- Radial Pressure Pulse Therapy Device — Guangzhou Longest Medical Technology Co., Ltd. · Class I
- CHATTANOOGA — Storz Medical AG · Class III
- Radial Pressure Pulse Therapy Device — Guangzhou Longest Science & Technology Co., Ltd. · Class I
- CHATTANOOGA — Storz Medical AG · Class III
- DUOLITH® — Storz Medical AG · Class III
Cleared under the same submission
K141332 also covers:
- 1-Level Cervical Plates, 20 mm — Captiva Spine
- 1-Level Cervical Plates, 22 mm — Captiva Spine
- 1-Level Cervical Plates, 24 mm — Captiva Spine
- 1-Level Cervical Plates, 26 mm — Captiva Spine
- 1-Level Cervical Plates, 28 mm — Captiva Spine
- 1-Level Cervical Plates, 30 mm — Captiva Spine
- 1-Level Cervical Plates, 32 mm — Captiva Spine
- 1-Level Cervical Plates, 34 mm — Captiva Spine
- 2-Level Cervical Plates, 36 mm — Captiva Spine
- 2-Level Cervical Plates, 38 mm — Captiva Spine
- 2-Level Cervical Plates, 40 mm — Captiva Spine
- 2-Level Cervical Plates, 42 mm — Captiva Spine
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
- Captiva Spine
Sources (1)
- FDA UDI 63749ba4-5793-48d2-879b-aa24bd6490ca 35 fields · synced May 31, 2026