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Infinty External Hex System

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
INFINTY EXTERNAL HEX SYSTEM FDA UDI
Generic Name
Screw endosteal dental implant, one-piece FDA UDI
Device Name
OCTOGON MULTI UNIT ABUTMENT SCREW AMGLED NARROW/REGULAR FDA UDI
Model / Reference
5033MUS FDA UDI
Description
OCTOGON MULTI UNIT ABUTMENT SCREW AMGLED NARROW/REGULAR FDA UDI

Identifiers

Catalog Number
5033MUS FDA UDI
Primary DI / UDI-DI
00614950027736 FDA UDI
510(k) Number
K103790 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, one-piece 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Screw endosteal dental implant, one-piece

Infinty External 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 Screw endosteal dental implant, one-piece.

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 9cbfdc03-8ef8-42e0-8c5b-055b4923419b 36 fields · synced Jun 7, 2026