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Intra-Lock

FDA UDI

Class II (US FDA UDI)

by Intra-Lock International

Identity

Trade Name
Intra-Lock FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
FlatTop Retaining Screw, FlatTop Implants FDA UDI
Model / Reference
FTRS FDA UDI
Description
FlatTop Retaining Screw, FlatTop Implants FDA UDI

Identifiers

Catalog Number
FTRS FDA UDI
Primary DI / UDI-DI
D742FTRS0 FDA UDI
510(k) Number
K130140 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant system 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

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

Category: Dental implant system

Intra-Lock by Intra-Lock International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

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 b0c2efb6-d142-40d6-965e-c291fd6c6542 35 fields · synced Jun 8, 2026