GreenMark Biomedical Lab

FDA Device Registration & Listing · Ann Arbor, MI, US · Registration 3020856747

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
3020856747
FEI Number
3020856747
Entity Name
GreenMark Biomedical Lab
City/State/Country
Ann Arbor, MI, US
Establishment Address
1600 Huron Parkway, Building 520, 2nd Floor, Ann Arbor, MI 48109, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GreenMark Biomedical Inc. (Owner Number: 10083206)
Owner / Operator Contact Address
325 E. Grand River Avenue, Suite 314, East Lansing, MI 48823, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K200601
PMA Number
N/A

All Registered Proprietary Names

CrystLCare LumiCare

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJR Agent, Polishing, Abrasive, Oral Cavity Dental Class 1 872.6030 2023-06-01
LFC Device, Caries Detection Dental Class 2 872.1740 2021-11-02
EAQ Detector, Ultraviolet Dental Class 2 872.6350 2021-11-02

Official Correspondent

Gregory Last

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GreenMark Biomedical 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
K121698 Dentsply International, Inc. NUPRO SENSODYNE PROPHYLAXIS PASTE WITH NOVAMIN 2012-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020856747. Last updated year: 2026. Please use registration number 3020856747 when referencing this establishment in official correspondence.
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