Manufacturer registered with FDA

Boyd Industries, Inc.

Clearwater, FL, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator9030301ManufacturerRepacker / relabeler

Device types listed: 3
Brands and models: 43
510(k) clearances: 12002–2002
Markets registered in: 23 registrations outside the US
Establishments: 1United States

510(k) clearances per year, 2000–2026

Registered in 2 markets

Where regulators' registries name Boyd Industries, Inc. as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Manufacturer	Boyd Industries, Inc.	1 clearances	2002–2002	Below
Taiwan	TFDA	Manufacturer	BOYD INDUSTRIES, INC.	3	2005–2007	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Boyd Industries, 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
Dental Operating LightEAZ · Class 1	Dental operating lights	Lister	C210C300 LED Examination LightC500 Camera Examination Light SystemC510 LED Examination LightC600 LED Examination LightS1900 LED Examination LightS200 LED Dental Surgery LightS300 LED Dental Surgery LightS4000 LED Examination LightSolarlite 900-1 Examination Light	2002
Operative Dental UnitEIA · Class 1	Dental chairs & operative units	Maker	CDU415CSU320CSU351CSU351SQCSU356CSU356SQCSU362CSU362SQCSU370SLCSU370SQ 1 more CSU456SQ	2009
Dental Chair without Operative UnitNRU · Class 1	Dental chairs & operative units	Maker	E3010CBE3010FBE3010LCE3010LSE5550E5550XM3000CBM3000FBM3000LCM3000LS 12 more M300XM3010CBM3010FBM3010LCM3010LSP3000LSS2601S2605S2614S2615S2914S3100LC	2014

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 Boyd Industries, Inc. as the applicant.

Decided	510(k)	Device	Device type
8 Aug 2002	K020833	BOYD DELIVERY UNIT	EIA Operative Dental Unit

Registered establishments

Establishment	Location	What it does
BOYD INDUSTRIES, INC.FDA reg. 1062917	CLEARWATER, FL, United States	Manufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9030301). 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.