AccessGUDID - DEVICE: Osteon Medical (D102SGKAA0)

GUDID

Device Identifier (DI) Information

Brand Name: Osteon Medical
Version or Model: 1
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: IMPLANT SOLUTIONS PTY LTD

Primary DI Number: D102SGKAA0
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 756242111 *Terms of Use

Device Description: Scan Gauge Kits are a selection of scan gauges, which are designed to facilitate the acquisition of accurate implant position readings in scans taken with intraoral scanners for full arch prosthetic restorations. The scan gauges are to be mounted directly on the implant abutment embedded in the patient’s mouth using the driver and screws provided in the kit.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
61641	Dental implant abutment analog, intraoral-scanning, single-use	An intraoral device intended to be used as a temporary copy of a dental implant abutment for attachment to a final dental implant and/or implant abutment during a scanning procedure to confirm its orientation/position as part of a dental restoration; it may in addition be intended for laboratory scanning. It is typically made of a radiopaque material (e.g., barium sulfate) and may be used in conjunction with an intraoral x-ray sensor. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NDP	Accessories, Implant, Dental, Endosseous

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: e2c594a1-990f-40ca-af1c-0180750a7d57
Public Version Date: February 06, 2025
Public Version Number: 2
DI Record Publish Date: December 19, 2022