Registered with FDA

Ortho-Cycle Co.

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

FDA owner/operator1052235Reprocessor

Device types listed: 1
Brands and models: 0
510(k) clearances: 11991–1991
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 1990–2026

Devices listed with FDA

What Ortho-Cycle Co. currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Orthodontic Metal BracketEJF · Class 1	Orthodontic brackets	Lister	—	2012

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 Ortho-Cycle Co. as the applicant.

Decided	510(k)	Device	Device type
27 Nov 1991	K913913	REFURBISHED ORTHODONTIC APPLIANCES	EJF Orthodontic Metal Bracket

Registered establishments

Establishment	Location	What it does
ORTHO-CYCLE CO.FDA reg. 1052235	HOLLYWOOD, FL, United States	Reprocessor

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1052235). 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.