Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1062917

FEI Number

3001239142

Entity Name

BOYD INDUSTRIES, INC.

City/State/Country

CLEARWATER, FL, US

Establishment Address

12900 44TH ST. NORTH, CLEARWATER, FL 33762, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BOYD INDUSTRIES, INC. (Owner Number: 9030301)

Owner / Operator Contact Address

12900 44TH ST. NORTH, --, Clearwater, FL 33762, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SMR Maxi Cabinet, Standard - Tall SMR Maxi Cabinet, Deluxe SMR Maxi Cabinet, Deluxe - Tall SMR Maxi Cabinet, Standard S1900 LED Examination Light C300 LED Examination Light S4000 LED Examination Light C210 S200 LED Dental Surgery Light C510 LED Examination Light C500 Camera Examination Light System S300 LED Dental Surgery Light Solarlite 900-1 Examination Light C600 LED Examination Light Solarlite 900-1 BOS - 310 Clinical Operator Stool BOS - 315 Clinical Operator Stool

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ETF	Unit, Examining/Treatment, Ent	Ear, Nose, Throat	Class 1	874.5300	2023-05-12
EAZ	Light, Operating, Dental	Dental	Class 1	872.4630	2002-04-10
KZF	Device, Medical Examination, Ac Powered	General Hospital	Class 1	880.6320	2023-05-12
INM	Chair, With Casters	Physical Medicine	Class 1	890.3100	2023-05-12

Official Correspondent

Adrian LaTrace

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BOYD INDUSTRIES, 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
K851742	Burton Medical Products Corp.	MEDICAL EXAMINATION LIGHTS	1985-05-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0011-2015	Nemschoff Chairs, Inc. 909 N 8th St 2218 Julson Ct Sheboygan WI 53081-4056	1	Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS: 792-12. Designed to provide patient comfort during patient treatment sessions. The chair may include a manual control reclining mechanism. Customer configurable models are also available. The Serenity III Exam 791-12E was discontinued 11/1/2010.
Z-0031-2013	Winco Mfg., LLC	1	Caremor Cliner"*Manufactured By WincoOcala, FL 34474 www.wincomfg.comModel No. 536 Serial No. 536A-101475" Literature: "Caremor Cliner 5351/5361WincoISO 9001-2008 CertifiedOur most comfortable and versatile reclinerEase of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.KEY FEATURE'SInfinite positioning backPadded armrests w/arm guardWebbed elastic suspension back and seatRemovable side panelsContinuous seat & legrest cushion5351 w/tray5361 w/out tray1.800.237.33775516 SW 1st LaneOcala, Florida 34474www.wincomfg.comProudly Made in the USA*" Patient recliner chair
Z-0032-2013	Winco Mfg., LLC	1	Caremor Cliner is labeled in part: "*Manufactured By WincoOcala, FL 34474 www.wincomfg.comModel No. 535 Serial No. 535A-104522" Literature: "Caremor Cliner 5351/5361WincoISO 9001-2008 CertifiedOur most comfortable and versatile reclinerEase of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.KEY FEATURE'SInfinite positioning backPadded armrests w/arm guardWebbed elastic suspension back and seatRemovable side panelsContinuous seat & legrest cushion5351 w/tray5361 w/out tray1.800.237.33775516 SW 1st LaneOcala, Florida 34474www.wincomfg.comProudly Made in the USA*" Patient recliner chair

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1062917. Last updated year: 2026. Please use registration number 1062917 when referencing this establishment in official correspondence.