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CERALOG PL Implant, Ø 5.0 L 11

FDA UDI

Class II (US FDA UDI)

by CeramTec Schweiz GmbH

Identity

Trade Name
CERALOG PL Implant, Ø 5.0 L 11 FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Dental Implant FDA UDI
Model / Reference
HP1040.5011 FDA UDI
Description
Dental Implant FDA UDI

Identifiers

Catalog Number
HP1040.5011 FDA UDI
Primary DI / UDI-DI
07640161396494 FDA UDI
510(k) Number
K163043 FDA UDI
K180184 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

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

Yes

FDA UDI

Category: Dental implant system

CERALOG PL Implant, Ø 5.0 L 11 by CeramTec Schweiz GmbH — 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 62cdb155-9cb1-4e43-8eff-96b2970c179f 36 fields · synced May 30, 2026