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OVC3 Hybrid

FDA UDI

Class II (US FDA UDI)

by Rhondium, Ltd.

Identity

Trade Name
OVC3 Hybrid FDA UDI
Generic Name
Preformed dental crown, permanent FDA UDI
Device Name
The OVC3 Hybrid Premolar Kit consists of a set of 12 OVCs in tooth shade A3 -one each for 4 premolar tooth types, in three sizes for each tooth type individually packaged. Each OVC Hybrid is packaged with 2 x OVC Wedges, 2 x Stretch Wedges, a Selector Key, 2 x OVC3 Matrix Band, 1 x Hex Stick, and an OVC Hybrid Replica. FDA UDI
Model / Reference
OVC3 Hybrid Premolar Kit A3 FDA UDI
Description
The OVC3 Hybrid Premolar Kit consists of a set of 12 OVCs in tooth shade A3 -one each for 4 premolar tooth types, in three sizes for each tooth type individually packaged. Each OVC Hybrid is packaged with 2 x OVC Wedges, 2 x Stretch Wedges, a Selector Key, 2 x OVC3 Matrix Band, 1 x Hex Stick, and an OVC Hybrid Replica. FDA UDI

Identifiers

Catalog Number
9421031795610 FDA UDI
Primary DI / UDI-DI
09421031795610 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Preformed dental crown, permanent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

OVC3 Hybrid by Rhondium, Ltd. — Class II — 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
Rhondium, Ltd.

Sources (1)

  • FDA UDI 8bcf4b6e-4ef4-471b-a4a2-6e32364fc771 38 fields · synced May 31, 2026