gudid Primary ID: IMPLATE Connector, 7mm x 10

Implate (UDI IMPLATE Connector, 7mm x 10)

Manufactured by SKELETAL DYNAMICS L.L.C.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Implate (Model/Catalog Number: IMPLATE Connector, 7mm x 10) is a medical device manufactured by SKELETAL DYNAMICS L.L.C.. This product is indexed under FDA Product Code / Category Classification HSP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: IMPLATE Connector, 7mm x 10
Product Code / EMDN: HSP
Device Name
Database Sync Date: 2026-08-09 09:39:24

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of Implate?

The registered manufacturer of record for Implate is SKELETAL DYNAMICS L.L.C..

What is the Primary UDI-DI identifier for Implate?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IMPLATE Connector, 7mm x 10.

What classification code is assigned to this device?

This device is registered under product classification code HSP.

Similar Classification Devices (HSP)

Other Devices by SKELETAL DYNAMICS L.L.C.

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