Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004513650

FEI Number

3004513650

Entity Name

RMAC SURGICAL INC

City/State/Country

Etobicoke Ontario, CA

Establishment Address

80 Galaxy Blvd, Unit 8, Etobicoke Ontario M9W4Y8, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RMAC Surgical Inc (Owner Number: 10028160)

Owner / Operator Contact Address

80 Galaxy Blvd, Unit 8, Etobicoke, CA-ON M9W4Y8, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PharmaTags PharmaTags: Sterile Med Label Kits Measurement Ruler

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FZZ	Marker, Skin	General, Plastic Surgery	Class 1	878.4660	2025-02-12
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2023-02-03
LYV	Label Or Tag, Sterile	General, Plastic Surgery	Class 1	878.4800	2009-01-05
FTY	Tape, Measuring, Rulers And Calipers	General, Plastic Surgery	Class 1	878.4800	2024-09-17

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

RMAC Surgical Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004513650. Last updated year: 2026. Please use registration number 3004513650 when referencing this establishment in official correspondence.