Company · FR

Luneau SA

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 2017. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
HKX	Tonometer, Ac-Powered	2
HJC	Esthesiometer, Ocular	1
HJK	Lens, Contact, Polymethylmethacrylate, Diagnostic	1
HKY	Tonometer, Manual	1

Decided	510(k)	Device and applicant	Code
Apr 24, 2017	K162067	VX130 Ophthalmic Diagnostic Device Luneau Sas, FR	HKX
Jun 1, 2015	K143086	VX120 Ophthalmic Diagnostic Device Luneau Sas, FR	HKX
Feb 20, 2003	K023838	LUNEAU STERILE TONOMETER SEPARATION PRISMS Luneau SA, FR	HKY
Sep 24, 2002	K022413	LUNEAU 3 MIRROR LENS Luneau SA, FR	HJK
May 30, 1985	K851557	ANESTHESIOMETER Luneau SA, FR	HJC

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