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CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus

FDA UDI

Class II (US FDA UDI)

by ALTATEC GmbH

Identity

Trade Name
CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus, d 3.3 mm, L 16 mm FDA UDI
Model / Reference
K1076.3316 FDA UDI
Description
CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus, d 3.3 mm, L 16 mm FDA UDI

Identifiers

Catalog Number
K1076.3316 FDA UDI
Primary DI / UDI-DI
E219K107633161 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.3 Millimeter FDA UDI
Length — 16 Millimeter FDA UDI

Category: Screw endosteal dental implant, two-piece

CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus by ALTATEC GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ALTATEC GmbH

Sources (1)

  • FDA UDI 39d8bea2-9ed3-4476-8a4a-39c352430536 36 fields · synced May 31, 2026