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Press Form Kit

FDA UDI

Class I (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
PRESS FORM KIT FDA UDI
Generic Name
Temporary dental crown/bridge FDA UDI
Device Name
PRESS FORM KIT, .020 SHEETS FDA UDI
Model / Reference
EPF172A FDA UDI
Description
PRESS FORM KIT, .020 SHEETS FDA UDI

Identifiers

Catalog Number
EPF172A FDA UDI
Primary DI / UDI-DI
00841494105129 FDA UDI
FDA Product Code
EBL FDA UDI
GMDN Term
Temporary dental crown/bridge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Temporary dental crown/bridge

Press Form Kit by Cynosure, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary dental crown/bridge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI 1b800e3f-333f-44b9-adb6-1c83ce47b634 34 fields · synced Jun 6, 2026