Data / Medical devices / United States / Boyd Industries, Inc.
Boyd Industries, Inc.: FDA-registered device maker in Clearwater, FL, United States, 1 510(k) clearance
Boyd Industries, Inc. is registered with the FDA (registration 1062917) in Clearwater, FL, United States. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 8, 2002. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1062917
- FEI number
- 3001239142
- Address
- 12900 44TH ST. North, Clearwater, FL, United States, 33762
- Owner or operator
- BOYD INDUSTRIES, INC. (9030301)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- April 10, 2002
- Registered through
- 2026
- Brand names listed
- BOS - 310 Clinical Operator Stool, BOS - 315 Clinical Operator Stool, C210, C300 LED Examination Light, C500 Camera Examination Light System, C510 LED Examination Light, C600 LED Examination Light, CDU415 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, Without Operative Unit | NRU | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Examination And Treatment | FRK | 1 | Manufacturer | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Manufacturer | accessdata.fda.gov |
| Device, Medical Examination, Ac Powered | KZF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Unit, Examining/Treatment, Ent | ETF | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 8, 2002 | K020833 | BOYD DELIVERY UNIT | EIA | Substantially Equivalent | Boyd Industries, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, Dental, Without Operative Unit
- All makers of Device, Medical Examination, Ac Powered
- All makers of Unit, Operative Dental
- All makers of Unit, Examining/Treatment, Ent
- All makers of Chair, With Casters
- All makers of Light, Operating, Dental
Updated August 8, 2002. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.