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Ditron Dental

FDA UDI

Class II (US FDA UDI)

by Ditron Dental Ltd

Identity

Trade Name
Ditron Dental FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
Conical Conn. Advanced Precision Implant ø4.20mm L11.5mm FDA UDI
Model / Reference
APC-42011 FDA UDI
Description
Conical Conn. Advanced Precision Implant ø4.20mm L11.5mm FDA UDI

Identifiers

Catalog Number
APC-42011 FDA UDI
Primary DI / UDI-DI
07290109288888 FDA UDI
510(k) Number
K243066 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 11.5 Millimeter FDA UDI
Outer Diameter — 4.20 Millimeter FDA UDI

Category: Screw endosteal dental implant, two-piece

Ditron Dental by Ditron Dental Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ditron Dental Ltd

Sources (1)

  • FDA UDI d09a3378-67b5-49f9-afa6-ccca7b4e4758 37 fields · synced May 30, 2026