Identity
- Trade Name
- Neuro & Craniofacial Fixation System FDA UDI
- Generic Name
- Orthopaedic implant driver FDA UDI
- Device Name
- Sterilized Electric Screw Driver, Cranial, Plastic, electronics, SST FDA UDI
- Model / Reference
- LS-572 FDA UDI
- Description
- Sterilized Electric Screw Driver, Cranial, Plastic, electronics, SST FDA UDI
Identifiers
- Primary DI / UDI-DI
- M711LS5720 FDA UDI
- 510(k) Number
- K101563 FDA UDI
- FDA Product Code
- KIJ FDA UDI
- GMDN Term
- Orthopaedic implant driver FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
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
Category: Orthopaedic implant driver
Neuro & Craniofacial Fixation System by Innovasis, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Innovasis, Inc.
Sources (1)
- FDA UDI a22aadab-27fb-4355-899b-42cffc20198e 35 fields · synced May 30, 2026