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Valence Robotic Navigation System

FDA UDI

Class II (US FDA UDI)

by Alphatec Spine, Inc.

Identity

Trade Name
Valence Robotic Navigation System FDA UDI
Generic Name
Surgical instrument guard, reusable FDA UDI
Device Name
Tissue Protector, M Smooth FDA UDI
Model / Reference
525-810 FDA UDI
Description
Tissue Protector, M Smooth FDA UDI

Identifiers

Primary DI / UDI-DI
00190376541358 FDA UDI
510(k) Number
K232413 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Surgical instrument guard, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument guard, reusable

Valence Robotic Navigation System by Alphatec Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument guard, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 53192e9b-b902-4f3d-8624-6bd0a2979556 35 fields · synced Jun 8, 2026