FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

Propex IQ Apex Locator

K Number: K191806 · Decision Oct 3, 2019
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
65
Review Days
90

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Propex IQ Apex Locator
K Number
K191806
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
July 5, 2019
Decision Date
October 3, 2019
Product Code
LQY
Advisory Committee
Unknown
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LQY Locator, Root Apex

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LQY), ordered by most recent decision date.

View all

Other Clearances by Dentsply Sirona

K Number Device Name
K260785 DS Core CBCT Anatomy
K253959 Primevision 3D
K252343 Atlantis® Abutments in Titanium
K252248 CEREC Tessera Abutment System
K251205 Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants
K250295 Dentsply Sirona Titanium Bases system
K250081 Atlantis® Abutments in Titanium
K242462 CEREC Cercon 4D CAD/CAM Blocks
K241557 Cercon® yo ML
K234018 CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System
Search all 65 clearances from Dentsply Sirona →