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Symmetry Ultra® Reveal

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Ultra® Reveal FDA UDI
Generic Name
Surgical retractor/retraction system blade, reusable FDA UDI
Device Name
Ultra Instruments® Retractor, Reveal Lumbar System, w/Sterilization Case FDA UDI
Model / Reference
59-1000S FDA UDI
Description
Ultra Instruments® Retractor, Reveal Lumbar System, w/Sterilization Case FDA UDI

Identifiers

Catalog Number
59-1000S FDA UDI
Primary DI / UDI-DI
00887482105061 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Surgical retractor/retraction system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retractor/retraction system blade, reusable

Symmetry Ultra® Reveal by Symmetry Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retractor/retraction system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI 96655490-8dca-4cc9-bba3-9fb6c662cc92 35 fields · synced May 31, 2026