KNIGHT DENTAL GROUP

FDA Device Registration & Listing · OLDSMAR, FL, US · Registration 3004883837

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004883837
FEI Number
3004883837
Entity Name
KNIGHT DENTAL GROUP
City/State/Country
OLDSMAR, FL, US
Establishment Address
3659 Tampa Rd, OLDSMAR, FL 34677, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Knight Dental Group (Owner Number: 9102879)
Owner / Operator Contact Address
3659 TAMPA ROAD, --, Oldsmar, FL 34677, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

porcelain fused to metal Preat Abutments PFM PFM Partial Restoration, Porcelain Denture

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NSJ Restoration, Noble Metal Unknown Class N N/A 2011-10-12
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2022-12-16
NSO Restoration, Porcelain-Fused-To-Metal Unknown Class N N/A 2011-10-12
NSQ Restoration, Base Metal Unknown Class N N/A 2011-10-12
NSK Dentures, Partial Unknown Class N N/A 2011-10-12
NSP Restoration, Porcelain Unknown Class N N/A 2011-10-12
NSL Dentures, Full Unknown Class N N/A 2011-10-12

Official Correspondent

Lonnie Lee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Knight Dental Group
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K211871 Faico Medical, LLC FAICO Dental Implant System and CAD/CAM Abutments 2021-11-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0007-2018 Implant Direct Sybron Manufacturing, LLC 2
Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.

Similar Registrations

Registration Number Establishment Name Location
3012821743 HONGKONG DS DENTAL TECHNOLOGY CO. LIMITED Tung Chung Lantau, HK
3004711948 PAN-AM DENTAL, INC. SAVANNAH, GA, US
3009795022 SHIMMER COMPUTERIZED DENTAL TECHNOLOGY CO.,LTD Zhuhai Guangdong, CN
3009488697 ZH GRACEFUL DENTAL LAB CO., LTD. Zhuhai Guangdong, CN
3007721975 KDN UijungBu Gyeonggi, KR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004883837. Last updated year: 2026. Please use registration number 3004883837 when referencing this establishment in official correspondence.
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