FDA Device Entity Profile: ACME UNITED CORP.

Known Identifiers & Locations

FEI Numbers 1030186, 3015544945, 3017482874, 3023917

Owner Operator Numbers 1217843

Locations Covered Keene, NH, US; North Salt Lake, UT, US; Rocky Mount, NC, US; VANCOUVER, WA, US

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1025972	ACME UNITED CORP.	Rocky Mount, NC, US	Repack or Relabel Medical Device	View Details
3015544945	Acme United Corporation - My Medic	North Salt Lake, UT, US	Repack or Relabel Medical Device	View Details
3017482874	LIVE SAFELY PRODUCTS, INC	Keene, NH, US	Repack or Relabel Medical Device	View Details
3023917	ACME UNITED CORP.	VANCOUVER, WA, US	Repack or Relabel Medical Device	View Details

510(k) Premarket Notifications (1)

Submission #	Device Name	Decision Date	Decision Description	Action
K833120	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29	Substantially Equivalent	View Details

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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