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Infinity Internal Hex System

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
Infinity Internal Hex System FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
infinity Internal 4.7 x 6.00 mm 4.5HD Hex Implant FDA UDI
Model / Reference
204706 FDA UDI
Description
infinity Internal 4.7 x 6.00 mm 4.5HD Hex Implant FDA UDI

Identifiers

Catalog Number
204706 FDA UDI
Primary DI / UDI-DI
00614950008254 FDA UDI
510(k) Number
K102981 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 6 Millimeter FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Infinity Internal Hex System by Ace Surgical Supply Co., Inc. — 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

Sources (1)

  • FDA UDI a084bf43-9504-47c0-a297-503373acb0ab 37 fields · synced Jun 8, 2026