Aptitude Anterior Cervical Plate System

FDA UDI

Class II (US FDA UDI)

by Curiteva, LLC

Identity

Trade Name: Aptitude Anterior Cervical Plate System FDA UDI
Generic Name: Manual orthopaedic bender, reusable FDA UDI
Device Name: Plate bender FDA UDI
Model / Reference: C155-200 FDA UDI
Description: Plate bender FDA UDI

Identifiers

Primary DI / UDI-DI: B648C1552000 FDA UDI
510(k) Number: K181549 FDA UDI
K181562 FDA UDI
FDA Product Code: KWQ FDA UDI
GMDN Term: Manual orthopaedic bender, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3060 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Manual orthopaedic bender, reusable

Aptitude Anterior Cervical Plate System by Curiteva, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Manual orthopaedic bender, reusable.

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CLAW CHARLOTTE — WRIGHT MEDICAL TECHNOLOGY, INC. · Class I

Cleared under the same submission

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 II	Pending data

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Manufacturer

Manufacturer: Curiteva, LLC

Sources (1)

FDA UDI d74129f3-7baa-438c-800e-f29a2e0c024c 35 fields · synced Jun 8, 2026