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Dynamik Intervertebral Body Fusion Device

FDA UDI

Class II (US FDA UDI)

by Spineart

Identity

Trade Name
Dynamik Intervertebral Body Fusion Device FDA UDI
Generic Name
Bone matrix implant, synthetic, non-antimicrobial FDA UDI
Device Name
Bone Substitute L22 H16 FDA UDI
Model / Reference
DYN-BS 22 16-S FDA UDI
Description
Bone Substitute L22 H16 FDA UDI

Identifiers

Catalog Number
DYN-BS 22 16-S FDA UDI
Primary DI / UDI-DI
07640139343819 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Bone matrix implant, synthetic, non-antimicrobial 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 22 Millimeter FDA UDI
Height — 12 Millimeter FDA UDI

Category: Bone matrix implant, synthetic, non-antimicrobial

Dynamik Intervertebral Body Fusion Device by Spineart — 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
Spineart

Sources (1)

  • FDA UDI b54167ce-5450-43b3-837e-167645f028a1 36 fields · synced Jun 1, 2026