• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Neodent GM x 4mm Healing Abutment

  • Print
  • Share
  • E-mail
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC

New Search Back to Search Results
  Class 2 Device Recall Neodent GM x 4mm Healing Abutment see related information
Date Initiated by Firm July 18, 2023
Date Posted October 24, 2023
Recall Status1 Open3, Classified
Recall Number Z-0153-2024
Recall Event ID 92867
510(K)Number K220823  
Product Classification Abutment, implant, dental, endosseous - Product Code NHA
Product Preat REF 9007123, Neodent GM x 4mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Code Information UDI-DI: 00842092161388/Lot #OF018357
Recalling Firm/
Preat Corp
2625 Skyway Dr Ste B
Santa Maria CA 93455-1405
For Additional Information Contact Nichole Fetterman
Manufacturer Reason
for Recall
The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage
FDA Determined
Cause 2
Process change control
Action On August 4, 2023, Preat Corporation issued a "Urgent Medical Device Recall" notification via: USPS. Preat ask consignees to take the following actions: Product within the scope of the recall shall be discarded or returned to Preat Corporation. Instructions for the return will be provided. Complete and email response form to Nichole Fetterman, E-Mail: nfetterman@younginnovations.com or mail to Preat Corporation, Attn. Nichole Fetterman, 2625 Skyway Drive, Ste. B, Santa Maria, CA 93455
Quantity in Commerce 23 units
Distribution US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: None
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = NHA and Original Applicant = Preat Corporation