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EZCrown

FDA UDI

Class I (US FDA UDI)

by Sprig Oral Health Technologies, Inc.

Identity

Trade Name
EZCrown FDA UDI
Generic Name
Preformed dental crown, temporary FDA UDI
Device Name
Sprig Posterior Crown -Mandibular Left Second Molar FDA UDI
Model / Reference
R-EZC-P-K6 FDA UDI
Description
Sprig Posterior Crown -Mandibular Left Second Molar FDA UDI

Identifiers

Primary DI / UDI-DI
00819235020765 FDA UDI
510(k) Number
K091362 FDA UDI
FDA Product Code
ELZ FDA UDI
GMDN Term
Preformed dental crown, temporary FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3330 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

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

Category: Preformed dental crown, temporary

EZCrown by Sprig Oral Health Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Preformed dental crown, temporary.

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 dcf542e7-c0ea-44b2-8e23-e37a0fb6ea16 34 fields · synced Jun 1, 2026