Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017482874

FEI Number

3017482874

Entity Name

LIVE SAFELY PRODUCTS, INC

City/State/Country

Keene, NH, US

Establishment Address

25 Forge St, Keene, NH 03431, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ACME UNITED CORP. (Owner Number: 1217843)

Owner / Operator Contact Address

1 Waterview Drive, Shelton, CT 06484, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
OHO	First Aid Kit Without Drug	General, Plastic Surgery	Class 1	878.4014	2017-06-29
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2017-05-31

Official Correspondent

Roberta Bloom

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ACME UNITED CORP.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3015544945	Acme United Corporation - My Medic	North Salt Lake, UT, US
3023917	ACME UNITED CORP.	VANCOUVER, WA, US
1025972	ACME UNITED CORP.	Rocky Mount, NC, US

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3007329149	MAJESTIC AEROTECH, INC	Tacoma, WA, US
3009576895	FRIENDSHIP INDUSTRIES	Harrisonburg, VA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017482874. Last updated year: 2026. Please use registration number 3017482874 when referencing this establishment in official correspondence.