SOAR Retractor System

FDA UDI

Class I (US FDA UDI)

by Spineology Inc.

Identity

Trade Name: SOAR Retractor System FDA UDI
Generic Name: Hand-held surgical retractor, reusable FDA UDI
Device Name: Modified SOAR Top Ring FDA UDI
Model / Reference: 102-49-17 FDA UDI
Description: Modified SOAR Top Ring FDA UDI

Identifiers

Catalog Number: 100-1307 FDA UDI
Primary DI / UDI-DI: M7401001307 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Hand-held surgical retractor, reusable

SOAR Retractor System by Spineology Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Spineology Inc.

Sources (1)

FDA UDI 36f0b5a3-e364-4762-992f-58fdbac1c7ba 35 fields · synced May 31, 2026