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Symbios®

FDA UDI

Class II (US FDA UDI)

by Dentsply Implants Manufacturing GmbH

Identity

Trade Name
SYMBIOS® FDA UDI
Generic Name
Pliable-polymer dental regeneration membrane, bioabsorbable, ligated FDA UDI
Device Name
OsteoShield® PTFE Non-Resorbable Membrane (25x30mm) FDA UDI
Model / Reference
USOSNRM2530 FDA UDI
Description
OsteoShield® PTFE Non-Resorbable Membrane (25x30mm) FDA UDI

Identifiers

Catalog Number
OSNRM2530 FDA UDI
Primary DI / UDI-DI
D716OSNRM25300 FDA UDI
FDA Product Code
LYC FDA UDI
GMDN Term
Pliable-polymer dental regeneration membrane, bioabsorbable, ligated 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: Pliable-polymer dental regeneration membrane, bioabsorbable, ligated

Symbios® by Dentsply Implants Manufacturing GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pliable-polymer dental regeneration membrane, bioabsorbable, ligated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply Implants Manufacturing GmbH

Sources (1)

  • FDA UDI 96606089-fd5e-4e82-b0a4-425b53a89db8 36 fields · synced May 30, 2026