← Back to catalogue

VerteGlide Spinal Growth Guidance System

FDA UDI

Class II (US FDA UDI)

by Orthopediatrics Corp.

Identity

Trade Name
VerteGlide Spinal Growth Guidance System FDA UDI
Generic Name
Orthopaedic fixation implant alignment tool FDA UDI
Device Name
VERTEGLIDE 5.5MM ROD BEND CHECKER FDA UDI
Model / Reference
01-1723-2500 FDA UDI
Description
VERTEGLIDE 5.5MM ROD BEND CHECKER FDA UDI

Identifiers

Catalog Number
01-1723-2500 FDA UDI
Primary DI / UDI-DI
00840194480208 FDA UDI
510(k) Number
K241816 FDA UDI
FDA Product Code
PGM FDA UDI
GMDN Term
Orthopaedic fixation implant alignment tool FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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
MRI Safety
MR Conditional FDA UDI

Category: Orthopaedic fixation implant alignment tool

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

Similar devices

Also classified as Orthopaedic fixation implant alignment tool.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 4c53ebc8-433e-4677-a3af-8a136c7f39b8 36 fields · synced May 31, 2026