ORTHO-CYCLE CO.

FDA Device Registration & Listing · HOLLYWOOD, FL, US · Registration 1052235

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1052235
FEI Number
1052235
Entity Name
ORTHO-CYCLE CO.
City/State/Country
HOLLYWOOD, FL, US
Establishment Address
2026 Scott St, HOLLYWOOD, FL 33020, US
Establishment Type(s)
Reprocess Single-Use Device
Owner / Operator
ORTHO-CYCLE CO. (Owner Number: 1052235)
Owner / Operator Contact Address
2026 SCOTT ST., --, Hollywood, FL 33020, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EJF Bracket, Metal, Orthodontic Dental Class 1 872.5410 2012-06-20

Official Correspondent

PETRE CIOARA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ORTHO-CYCLE CO.
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
K894358 Ormco Corp. LUMINA ORTHODONTIC BRACKET 1989-09-15
K925012 American Orthodontics PLASTIC CHAIN 1993-09-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1052235. Last updated year: 2026. Please use registration number 1052235 when referencing this establishment in official correspondence.
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