RICOmed Manufacturing

FDA Device Registration & Listing · Richardson, TX, US · Registration 3007320533

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
3007320533
FEI Number
3007320533
Entity Name
RICOmed Manufacturing
City/State/Country
Richardson, TX, US
Establishment Address
1126 Alpine Dr, Richardson, TX 75080, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Repack or Relabel Medical Device
Owner / Operator
RICOCHET INDUSTRIES, INC. (Owner Number: 9068902)
Owner / Operator Contact Address
1126 Alpine Drive, Richardson, TX 75080, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RICOmed preformed wires

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZN Instruments, Dental Hand Dental Class 1 872.4565 2019-03-31
EHP Clasp, Preformed Dental Class 1 872.3285 2019-04-04
DZC Wire, Orthodontic Dental Class 1 872.5410 2019-04-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RICOCHET 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
K112640 Ormco Corp. HYPERELASTIC WIRE 2011-11-16

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007320533. Last updated year: 2026. Please use registration number 3007320533 when referencing this establishment in official correspondence.
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