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Ipd

FDA UDI

Class II (US FDA UDI)

by Implant Protesis Dental 2004 Sl

Identity

Trade Name
IPD FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Custom Ti Base Engaging Ø 3,6 H 0.5 FDA UDI
Model / Reference
INC3D FDA UDI
Description
Custom Ti Base Engaging Ø 3,6 H 0.5 FDA UDI

Identifiers

Catalog Number
IPD/EB-IN-00/3D FDA UDI
Primary DI / UDI-DI
08435566611544 FDA UDI
510(k) Number
K240570 FDA UDI
FDA Product Code
PNP FDA UDI
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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Ipd by Implant Protesis Dental 2004 Sl — 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 e9a007a4-7920-4199-9cdc-4128a53fc5ba 36 fields · synced May 30, 2026