SAFECROSS FIRST AID LTD.

FDA Device Registration & Listing · TORONTO Ontario, CA · Registration 9680884

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
9680884
FEI Number
3009964652
Entity Name
SAFECROSS FIRST AID LTD.
City/State/Country
TORONTO Ontario, CA
Establishment Address
21 KODIAK CRESCENT, TORONTO Ontario M3J 3E5, CA
Establishment Type(s)
Foreign Private Label Distributor
Owner / Operator
SAFECROSS FIRST AID LTD. (Owner Number: 9012132)
Owner / Operator Contact Address
21 KODIAK CRESCENT, --, TORONTO, ONTARIO, CA-ON M3J 3E5, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

FAK2 and FAK5, Basic, 25 Person, FAK1, 10 Person, 35 Person and 50 Person adhesive, Tape and bandage

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRR First Aid Kit With Drug Unknown Class N N/A 2007-11-23
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2014-02-18

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

SAFECROSS FIRST AID LTD.
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680884. Last updated year: 2026. Please use registration number 9680884 when referencing this establishment in official correspondence.
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