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Fortera

FDA UDI

Class II (US FDA UDI)

by Vivorte, Inc

Identity

Trade Name
Fortera FDA UDI
Generic Name
Bone matrix implant, synthetic, non-antimicrobial FDA UDI
Device Name
Calcium compound bone void filler (3 cc) FDA UDI
Model / Reference
3 cc FDA UDI
Description
Calcium compound bone void filler (3 cc) FDA UDI

Identifiers

Catalog Number
131133-03-S FDA UDI
Primary DI / UDI-DI
00868201000164 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone matrix implant, synthetic, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 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

Category: Bone matrix implant, synthetic, non-antimicrobial

Fortera by Vivorte, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, synthetic, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vivorte, Inc

Sources (1)

  • FDA UDI 69afa6f6-dcb7-4468-98bb-3a1c8af254b1 35 fields · synced May 30, 2026