AccessGUDID - DEVICE: Preat Implant Prosthetics (00842092175064)

GUDID

Device Identifier (DI) Information

Brand Name: Preat Implant Prosthetics
Version or Model: 9005767
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 9005767
Company Name: Preat Corporation

Primary DI Number: 00842092175064
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 117776048 *Terms of Use

Device Description: Keystone TiLobe®-compatible 3.5mm Titanium Blank Kit contains: 1 Keystone TiLobe®-compatible 3.5mm Titanium Blank 2 Keystone TiLobe®-compatible 3.5mm/4.1mm/5.0mm Titanium Screws

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
44879	Dental implant suprastructure, permanent, preformed	A prefabricated device intended to provide a permanent intermediate fixture level between a dental implant and the final prosthesis/restoration (e.g., bridge, single tooth, overdenture). It includes one or more structural component(s) [e.g., abutment, ball, bar, bar overlay, coping, ring], and may be made of various materials [e.g., titanium (Ti), plastic, gold alloy]. It includes devices glued to prostheses and/or devices that can be replaced during cleaning cycles. An abutment screw(s) may be included, however the suprastructure does not represent the screw(s) in isolation. It may also be referred to as an abutment assembly or mesostructure.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
NHA	Abutment, Implant, Dental, Endosseous
PNP	Dental Abutment Design Software For Dental Laboratory

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K220823	000

Device Exempt from Premarket Submission: No 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: 0de23468-72ef-4e2f-a6ed-01e3349f65f2
Public Version Date: June 27, 2025
Public Version Number: 6
DI Record Publish Date: November 01, 2022