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Photodynamic Bone Stabilization System

FDA UDI

by Illuminoss Medical Inc.

Identity

Trade Name
Photodynamic Bone Stabilization System FDA UDI
Generic Name
General-purpose light source FDA UDI
Device Name
Photodynamic Bone Stabilization LED Light Box FDA UDI
Model / Reference
SY210001 FDA UDI
Description
Photodynamic Bone Stabilization LED Light Box FDA UDI

Identifiers

Catalog Number
SY-2100-01 FDA UDI
Primary DI / UDI-DI
M986SY2100010 FDA UDI
GMDN Term
General-purpose light source FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: General-purpose light source

Photodynamic Bone Stabilization System by Illuminoss Medical Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose light source.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4a9ee3e2-3dac-4f63-9bad-e5e3e8fc08ea 34 fields · synced Jun 8, 2026