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Leforte Neuro System Bone Plate

FDA UDI

Class II (US FDA UDI)

by Jeil Medical Corporation

Identity

Trade Name
Leforte Neuro System Bone Plate FDA UDI
Generic Name
Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI
Model / Reference
N12-GP-020S FDA UDI

Identifiers

Primary DI / UDI-DI
08809265155577 FDA UDI
510(k) Number
K091679 FDA UDI
K103778 FDA UDI
K112812 FDA UDI
K141452 FDA UDI
FDA Product Code
JEY FDA UDI
HBW FDA UDI
GXR FDA UDI
GWO FDA UDI
GMDN Term
Craniofacial fixation plate, non-bioabsorbable, non-customized FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 FDA UDI
882.5360 FDA UDI
882.5250 FDA UDI
882.5320 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial fixation plate, non-bioabsorbable, non-customized

Leforte Neuro System Bone Plate by Jeil Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial fixation plate, non-bioabsorbable, non-customized.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b0944293-29af-4446-852e-49656c95212a 33 fields · synced May 29, 2026