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Straumann Granules

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
STRAUMANN GRANULES FDA UDI
Generic Name
Dental bone matrix implant, synthetic FDA UDI
Device Name
Straumann® BoneCeramic™ 500-1000 micrometer, 1.0 g FDA UDI
Model / Reference
BoneCeramic FDA UDI
Description
Straumann® BoneCeramic™ 500-1000 micrometer, 1.0 g FDA UDI

Identifiers

Catalog Number
070.205 FDA UDI
Primary DI / UDI-DI
07630031700179 FDA UDI
510(k) Number
K040646 FDA UDI
FDA Product Code
LYC FDA UDI
GMDN Term
Dental bone matrix implant, synthetic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 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

No

FDA UDI

Category: Dental bone matrix implant, synthetic

Straumann Granules by Institut Straumann SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental bone matrix implant, synthetic.

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 531b5713-6a40-45ac-aede-4809e577fff7 38 fields · synced Jun 6, 2026