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Cobalt Chrome Non Indexed UCLA Casting Abutment

FDA UDI

Class II (US FDA UDI)

by Surgikor, LLC

Identity

Trade Name
Cobalt Chrome Non Indexed UCLA Casting Abutment FDA UDI
Generic Name
Basket endosteal dental implant, two-piece FDA UDI
Device Name
3.75mm x L 11.0mm, Hex Connection, Regular Platform FDA UDI
Model / Reference
CORH FDA UDI
Description
3.75mm x L 11.0mm, Hex Connection, Regular Platform FDA UDI

Identifiers

Primary DI / UDI-DI
D824CORH0 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Basket endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Basket endosteal dental implant, two-piece

Cobalt Chrome Non Indexed UCLA Casting Abutment by Surgikor, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basket endosteal dental implant, two-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgikor, LLC

Sources (1)

  • FDA UDI 1f554c8e-6bd6-4aa8-a0ca-eb87d6581aed 33 fields · synced Jun 8, 2026