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REICHERT INC.

Last updated September 17, 2026

Information

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Device	Model / Reference	Registries	Class	Status
Atp (auto Non-Contact Tonometer/Pachymeter)	K042831	FDA 510(k)	Class II	Active
Tono-Vera® Tonometer and Ocu-Dot® Tonometer Probes (16305, 16306, 16318)	K233516	FDA 510(k)	Class II	Active
Ocular Response Analyzer	K081756	FDA 510(k)	Class II	Active
Soct Copernicus, Model 15205	K071839	FDA 510(k)	Class II	Active
Modification To: Ocu-Film Tip Cover	K070534	FDA 510(k)	Class II	Active
Xcel 455 Slit Lamp	K141954	FDA 510(k)	Class II	Active
Psl Portable Slit Lamp	K061330	FDA 510(k)	Class II	Active
Xcel 255 Slit Lamp	K063750	FDA 510(k)	Class II	Active

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Feb 28, 2025	Z-1501-2025	—	open, classified	The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Feb 28, 2025	Z-1500-2025	—	open, classified	The head of the phoropter head could come loose and potentially detach due to a default in the assembly.
Jul 20, 2023	Z-2512-2023	—	open, classified	Phoroptor VRx Head may detach from the bracket that connects the Phoroptor VRx Head to an ophthalmic stand. If the Phoroptor VRx Head detaches from the bracket, it can fall onto a patient or device operator