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Conhex

FDA UDI

Class II (US FDA UDI)

by Bhi Implants Ltd

Identity

Trade Name
CONHEX FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Ball Attachment Angled 40°-3mm Length Regular 2.42 Internal Hex FDA UDI
Model / Reference
1 FDA UDI
Description
Ball Attachment Angled 40°-3mm Length Regular 2.42 Internal Hex FDA UDI

Identifiers

Catalog Number
ABA4003 FDA UDI
Primary DI / UDI-DI
07290109743806 FDA UDI
510(k) Number
K103280 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 3 Millimeter FDA UDI
Angle — 40 degree FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Conhex by Bhi Implants Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bhi Implants Ltd

Sources (1)

  • FDA UDI 6a6b1068-0685-4bea-a3e3-59f4ddc3c891 38 fields · synced May 30, 2026