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VerteGlide Spinal Growth Guidance System

FDA UDI

Class I (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name
VerteGlide Spinal Growth Guidance System FDA UDI
Generic Name
Orthopaedic rod reducer FDA UDI
Device Name
VERTEGLIDE REVERSE ACTION ROCKER FDA UDI
Model / Reference
01-1720-0275 FDA UDI
Description
VERTEGLIDE REVERSE ACTION ROCKER FDA UDI

Identifiers

Catalog Number
01-1720-0275 FDA UDI
Primary DI / UDI-DI
00840194480109 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic rod reducer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic rod reducer

VerteGlide Spinal Growth Guidance System by Orthopediatrics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic rod reducer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthopediatrics Corp.

Sources (1)

  • FDA UDI 9018edfb-f2a2-4d30-9dbc-e5954a016a1a 35 fields · synced May 30, 2026