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Biotanium

FDA UDI

Class II (US FDA UDI)

by Basic Dental Implant Systems, Inc.

Identity

Trade Name
BIOTANIUM FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
4.5mm X 9mm Implant FDA UDI
Model / Reference
O4509S FDA UDI
Description
4.5mm X 9mm Implant FDA UDI

Identifiers

Primary DI / UDI-DI
00810123450060 FDA UDI
510(k) Number
K082749 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

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Category: Dental implant system

Biotanium by Basic Dental Implant Systems, Inc. — 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 c961723e-0797-4531-8007-3d9eaf44ff2c 34 fields · synced Jun 8, 2026