gudid Primary ID: 770-150

PRECISE HA LITE PARTIAL (UDI 770-150)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PRECISE HA LITE PARTIAL (Model/Catalog Number: 770-150) is a medical device manufactured by Grace Medical, Inc.. This product is indexed under FDA Product Code / Category Classification ETB within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2308-2026 View Full Alert →

TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis...

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Technical Specifications

Model Number: 770-150
Product Code / EMDN: ETB
Device Name: PRECISE HA LITE PARTIAL 1.50MM LENGTH HA/TITANIUM
Database Sync Date: 2026-08-09 09:59:39

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 PRECISE HA LITE PARTIAL?

The registered manufacturer of record for PRECISE HA LITE PARTIAL is Grace Medical, Inc..

What is the Primary UDI-DI identifier for PRECISE HA LITE PARTIAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 770-150.

What classification code is assigned to this device?

This device is registered under product classification code ETB.

Similar Classification Devices (ETB)

Other Devices by Grace Medical, Inc.

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