gudid Primary ID: TKR.IN.1332

Apollo Knee (UDI TKR.IN.1332)

Manufactured by CORIN LTD

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Apollo Knee (Model/Catalog Number: TKR.IN.1332) is a medical device manufactured by CORIN LTD. This product is indexed under FDA Product Code / Category Classification OLO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TKR.IN.1332
Product Code / EMDN: OLO
Device Name: Cortical bone Screw 3.2mm x 110mm
Database Sync Date: 2026-08-09 09:08:10

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Apollo Knee?

The registered manufacturer of record for Apollo Knee is CORIN LTD.

What is the Primary UDI-DI identifier for Apollo Knee?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TKR.IN.1332.

What classification code is assigned to this device?

This device is registered under product classification code OLO.

Similar Classification Devices (OLO)

Other Devices by CORIN LTD

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint