Company · US

Medicore, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 2021. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	2
JOM	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic	2
FMF	Syringe, Piston	1
LHQ	System, Telethermographic (Adjunctive Use)	1

Decided	510(k)	Device and applicant	Code
Sep 13, 2021	K212412	IRIS-XP Medicore Co., Ltd., KR	LHQ
Jun 13, 2011	K110374	MAX PULSE SYSTEM Medicore Co., Ltd., KR	JOM
Nov 29, 2007	K073323	SA-3000P Medicore Co., Ltd., KR	JOM
Feb 9, 1999	K983430	LITE-TOUCH SYRINGE Medicore, Inc.	FMF
Mar 21, 1988	K880869	MEDI-LET Medicore, Inc.	FMK
Mar 26, 1981	K810681	MEDI-LANCE Medicore, Inc.	FMK

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.