Device
Trial - Standard Baseplate
Manufacturer
Restor3d, Inc.
Model: 5500-4501 DI: 00840097535968 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: No Rx: Yes OTC: No
First Published: 2026-05-14 Current Version: 2026-05-22
Description
Trial - Standard Baseplate
Sterilization
Method Types - Sterilization Method: Moist Heat or Steam Sterilization
Device Sterile: No
Sterilization Prior To Use: Yes
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: 29276ef6-af9e-4684-9cd0-d892561c94b1
Distribution Status: In Commercial Distribution
DUNS Number: 080819836
Device Count: 1
DM Exempt: No
Premarket Exempt: No
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: No
Serial Number Tracked: Yes
Manufacturing Date Tracked: No
Expiration Date Tracked: No
Donation ID Number Tracked: No
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Device ID: 00840097535968
Type: Primary
Issuing Agency: GS1
GMDN
Code: 61246
Name: Surgical implant/trial-implant/sizer holder, single-use
Definition:
A hand-held manual surgical instrument designed to connect to and hold an implant (e.g., bone screw, bone graft), trial implant, or implantable device sizer/template (e.g., glenoid defect sizer, hearing implant template) to facilitate guidance, gauging/sizing, and/or monitoring of the held device during orthopaedic or ear/nose/throat (ENT) surgery. The instrument is typically made of metal or synthetic polymer materials and is typically constructed in the form of a long shaft with a handle at the proximal end and a device holding/fixation mechanism at the distal end. This is a single-use device.
FDA Product Codes
PHX
Shoulder Prosthesis, Reverse Configuration
Premarket Submissions
Submission Number: K243643
Supplement Number: 000