Manufacturer registered with FDA
GreenMark Biomedical Inc.
East Lansing, MI, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.
- Device types listed
- 3
- Brands and models
- 3
- 510(k) clearances
- 22021–2025
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 2007–2026
Devices listed with FDA
What GreenMark Biomedical Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Ultraviolet DetectorEAQ · Class 2 | — | Maker | LumiCare | 2021 |
| Oral Cavity Abrasive Polishing AgentEJR · Class 1 | Polishing & prophylaxis | Maker | CrystLCare | 2023 |
| Caries Detection DeviceLFC · Class 2 | Caries detection devices | Maker | LumiCare | 2021 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names GreenMark Biomedical Inc. as the applicant, including filings under its other names.
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| GreenMark Biomedical LabFDA reg. 3020856747 | Ann Arbor, MI, United States | Manufacturer |
Other names on FDA records
GreenMark Biomedical Lab
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10083206). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.