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Favo

FDA UDI

Class II (US FDA UDI)

by Silony Medical GmbH

Identity

Trade Name
FAVO FDA UDI
Generic Name
Metallic spinal interbody fusion cage FDA UDI
Device Name
FAVO S-TLIF Cage, 07x11x28mm, 0° FDA UDI
Model / Reference
S-FST-07112800-S FDA UDI
Description
FAVO S-TLIF Cage, 07x11x28mm, 0° FDA UDI

Identifiers

Catalog Number
S-FST-07112800-S FDA UDI
Primary DI / UDI-DI
04054896062020 FDA UDI
FDA Product Code
MAX FDA UDI
PHM FDA UDI
GMDN Term
Metallic spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

Dimensions & Sizes

Size
Height — 7 Millimeter FDA UDI
Width — 11 Millimeter FDA UDI
Length — 28 Millimeter FDA UDI
Angle — 0 degree FDA UDI

Category: Metallic spinal interbody fusion cage

Favo by Silony Medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Metallic spinal interbody fusion cage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Silony Medical GmbH

Sources (1)

  • FDA UDI 33651d87-1642-4b98-ac57-8b803774dd6e 35 fields · synced May 31, 2026