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Equator Abutment, Φ 6.5mm, GH 2mm

FDA UDI

Class II (US FDA UDI)

by BIO CONCEPT Co., Ltd.

Identity

Trade Name
Equator Abutment,Φ 6.5mm,GH 2mm FDA UDI
Generic Name
Dental implant system FDA UDI
Model / Reference
034220-1 FDA UDI

Identifiers

Primary DI / UDI-DI
06947600302889 FDA UDI
510(k) Number
K150388 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant system 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

Equator Abutment, Φ 6.5mm, GH 2mm by BIO CONCEPT Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

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 28ec0316-90a6-4d4b-b56e-b94ea7eac3fe 33 fields · synced May 31, 2026