CLEARTOOTH ELECTRONICS, INC.

FDA Device Registration & Listing · Boulder, CO, US · Registration 3008313821

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
3008313821
FEI Number
3008313821
Entity Name
CLEARTOOTH ELECTRONICS, INC.
City/State/Country
Boulder, CO, US
Establishment Address
106 Mineola Ct., Boulder, CO 80303, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Cleartooth Electronics, Inc. (Owner Number: 10031351)
Owner / Operator Contact Address
106 Mineola Ct., Boulder, CO 80303, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K033147
PMA Number
N/A

All Registered Proprietary Names

Cleartooth Digital X-Ray

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MUH System, X-Ray, Extraoral Source, Digital Dental Class 2 872.1800 2010-01-19

Official Correspondent

Scott Siegel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cleartooth Electronics, Inc.
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
K221008 Shanghai Handy Medical Equipment Co., Ltd. HDR Sensor- HDR361 (Size 1), HDR Sensor- HDR461 (Size 2) 2022-06-22
K160788 Ray Co., Ltd. RIOScan (RPS500) 2016-04-15

Similar Registrations

Registration Number Establishment Name Location
3042046320 QPIX SOLUTIONS, INC. Morrisville, NC, US
3020117925 ATHLOS OY Espoo Uusimaa, FI
2032641 CYBER MEDICAL IMAGING, INC. Los Angeles, CA, US
3004706313 VATECH CO., LTD. Hwaseong-si Gyeonggi, KR
3010281549 J. MORITA MFG. CORP., TOTTORI FACTORY Kurayoshi Tottori, JP
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008313821. Last updated year: 2026. Please use registration number 3008313821 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.