Magicare Tech Corp

FDA Device Registration & Listing · Ontario, CA, US · Registration 3016759113

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
3016759113
FEI Number
3016759113
Entity Name
Magicare Tech Corp
City/State/Country
Ontario, CA, US
Establishment Address
1940 E Locust St Ste A, Ontario, CA 91761, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Cecilia Tech Inc (Owner Number: 10068646)
Owner / Operator Contact Address
4290 E. Brickell St., Unit C, Ontario, CA 91761, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K203152
PMA Number
N/A

All Registered Proprietary Names

MagiCare

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2022-09-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cecilia Tech 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
K201622 Guangdong Kingfa Sci. & Tech.Co., Ltd. Medical surgical mask 2020-11-24
K881618 3M Company ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK 1988-05-09

Similar Registrations

Registration Number Establishment Name Location
3016247944 HYGENIX HEALTH SOLUTIONS LLC Torrance, CA, US
3016765490 XIAMEN CHUANFUTANG PHARMACEUTICAL CO.,LTD xiamen Fujian, CN
3018382937 MID-AMERICA SAFETY CORP Elk Grove Village, IL, US
3017598017 DURIO PPE SDN. BHD. Johor Bahru, MY
3002813051 IRIS USA INC Pleasant Prairie, WI, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016759113. Last updated year: 2026. Please use registration number 3016759113 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.