Identity
- Trade Name
- CyclaPlex Drill Guide FDA UDI
- Generic Name
- Orthopaedic implant aiming/guiding block attachment tool FDA UDI
- Device Name
- The CyclaPlex Drill Guide is a “H arm” device intended to guide drill bits at the right points and required drilling angles in the 1st and 2nd metatarsal bones. FDA UDI
- Model / Reference
- V7 FDA UDI
- Description
- The CyclaPlex Drill Guide is a “H arm” device intended to guide drill bits at the right points and required drilling angles in the 1st and 2nd metatarsal bones. FDA UDI
Identifiers
- Catalog Number
- DG-9201 FDA UDI
- Primary DI / UDI-DI
- 07290017626192 FDA UDI
- 510(k) Number
- K183094 FDA UDI
- FDA Product Code
- HTN FDA UDI
- GMDN Term
- Orthopaedic implant aiming/guiding block attachment tool 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic implant aiming/guiding block attachment tool
CyclaPlex Drill Guide by Alphamet Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
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
- Alphamet Ltd
Sources (1)
- FDA UDI 8bfbc4d9-aaad-4abd-aa41-f35fe3ce857e 36 fields · synced May 30, 2026