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Directcrown

FDA UDI

Class II (US FDA UDI)

by Direct Crown Products

Identity

Trade Name
DIRECTCROWN FDA UDI
Generic Name
Dental bridge, polymer FDA UDI
Device Name
ADULT POLYCARBONATE POSTERIOR BRIDGE KIT CONTAINING 1OZ ACRYLIC LIQUID, 1OZ ACRYLIC POWDER AND 16 BRIDGE CROWN SHELLS SIZES 1-8 OPAQUE FDA UDI
Model / Reference
PB FDA UDI
Description
ADULT POLYCARBONATE POSTERIOR BRIDGE KIT CONTAINING 1OZ ACRYLIC LIQUID, 1OZ ACRYLIC POWDER AND 16 BRIDGE CROWN SHELLS SIZES 1-8 OPAQUE FDA UDI

Identifiers

Primary DI / UDI-DI
D752PB3 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Dental bridge, polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Dental bridge, polymer

Directcrown by Direct Crown Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental bridge, polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9753731e-2d50-408b-8a50-369b8f1bcd8d 34 fields · synced May 30, 2026