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InterOss®

EUDAMEDFDA UDI

Class III (EU MDR)

Ref IOLGS050

by SigmaGraft Inc.

Identity

Trade Name
InterOss® EUDAMEDFDA UDI
Generic Name
Dental bone matrix implant, animal-derived FDA UDI
Device Name
InterOss® EUDAMED
Model / Reference
IOLGS050 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00852072007124 EUDAMEDFDA UDI
Basic UDI-DI
B-00852072007124 EUDAMED
510(k) Number
K151209 FDA UDI
FDA Product Code
NPM FDA UDI
EMDN Code
Q010302 DENTAL GRAFT DEVICES EUDAMED
GMDN Term
Dental bone matrix implant, animal-derived FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
872.3930 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

InterOss® by Sigmagraft, Inc. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SigmaGraft Inc.
EUDAMED SRN
US-MF-000015980
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 1aa190f8-e862-40f4-af08-285130cc835a 61 fields · synced Jul 26, 2026
  • FDA UDI e366484b-6317-465d-a571-41efce4cae38 35 fields · synced May 30, 2026