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Symmetry Facial Plane Relator Trial Kit

FDA UDI

Class II (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Symmetry Facial Plane Relator Trial Kit FDA UDI
Generic Name
Bite registration rim FDA UDI
Device Name
Bite registration rim FDA UDI
Model / Reference
051904 FDA UDI
Description
Bite registration rim FDA UDI

Identifiers

Catalog Number
051904 FDA UDI
Primary DI / UDI-DI
00359883002909 FDA UDI
FDA Product Code
ELW FDA UDI
EID FDA UDI
EHY FDA UDI
GMDN Term
Bite registration rim FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 FDA UDI
872.4565 FDA UDI
872.6880 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bite registration rim

Symmetry Facial Plane Relator Trial Kit by Den-Mat Holdings, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bite registration rim.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Den-Mat Holdings, LLC

Sources (1)

  • FDA UDI 39c2d66c-f6f2-444d-b3f5-26a322da1a76 36 fields · synced Jun 9, 2026