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50mm Stock TMJ Condylar Prosthesis (LEFT SIDE and RIGHT SIDE)

FDA UDI

Class III (US FDA UDI)

by Nexus Cmf, L.L.C.

Identity

Trade Name
50mm Stock TMJ Condylar Prosthesis (LEFT SIDE and RIGHT SIDE) FDA UDI
Generic Name
Mandibular condyle prosthesis FDA UDI
Device Name
50mm Stock TMJ Condylar Prosthesis (LEFT SIDE and RIGHT SIDE) FDA UDI
Model / Reference
500091 FDA UDI
Description
50mm Stock TMJ Condylar Prosthesis (LEFT SIDE and RIGHT SIDE) FDA UDI

Identifiers

Primary DI / UDI-DI
M9575000910 FDA UDI
FDA Product Code
LZD FDA UDI
GMDN Term
Mandibular condyle prosthesis FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
872.3940 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

50mm Stock TMJ Condylar Prosthesis (LEFT SIDE and RIGHT SIDE) by Nexus Cmf, L.L.C. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nexus Cmf, L.L.C.

Sources (1)

  • FDA UDI 31413149-90f8-4443-9bfb-56952cc3c3a8 34 fields · synced Jun 8, 2026