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MED LOGICS INC

United States·US-MF-000004600

Last updated May 25, 2026

What MED LOGICS INC makes

Med Logics Inc manufactures single-use keratome blades for corneal surgery, including models with specific dioptric power adjustments such as Plus 20, Minus 20, and Plano variants. Their portfolio also includes corneal cannulas, which are used in procedures like Descemet’s stripping endothelial keratoplasty (DSEK) and penetrating keratoplasty.

The company’s devices are classified under FDA categories including Class I, Class II, Class IIa, and Class IIb, with corresponding entries in the FDA’s 510(k) and UDI registries. They are also listed in the EU’s eudamed database, reflecting their distribution in both US and European markets.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Med Logics Inc manufacture?

Med Logics Inc specializes in single-use keratome blades and corneal cannulas. Their keratome blades are designed for corneal surgery, including variants with specific dioptric power adjustments like Plus 20, Minus 20, and Plano. The cannulas are used in procedures such as Descemet’s stripping endothelial keratoplasty (DSEK) and penetrating keratoplasty.

Where is Med Logics Inc based?

Med Logics Inc is based in the United States. Their devices are distributed in both US and European markets, as evidenced by their listings in the FDA and EU’s eudamed databases.

Which regulatory registries list Med Logics Inc’s devices?

Med Logics Inc’s devices are listed in the FDA’s 510(k) and UDI registries, as well as the EU’s eudamed database. These listings reflect their regulatory compliance and market distribution in both the US and Europe.

How are Med Logics Inc’s devices classified under FDA regulations?

Med Logics Inc’s devices fall under FDA classification categories including Class I, Class II, Class IIa, and Class IIb. The classification depends on the device’s intended use and risk level, with higher classes (e.g., Class IIb) typically requiring more stringent regulatory scrutiny due to increased risk.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: United States
Address: 1627 Enterprise Street, Athens, United States
Website: www.mlogics.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 9495823891
PRRC Contact: Justin Ross
EUDAMED SRN: US-MF-000004600
FDA FEI Number: —
DUNS Number: 075390489

Catalogue (106)

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Device	Model / Reference	Registries	Class	Status
Clb®	ML7030 (-30)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7100 (-20)	EUDAMEDFDA UDI	Class IIa	Active
ML7 Sterilization Tray	1500ML7	EUDAMEDFDA UDI	Class IIa	Active
ML7 Vacuum Handle	1300ML7	EUDAMEDFDA UDI	Class IIa	Active
Vacuum Ring; 9.0mm	1090ML7	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP6S0SP-23030S	EUDAMED	Class IIa	Active
ML7 Head; 100µm	0100ML7	EUDAMEDFDA UDI	Class IIa	Active
Vacuum Ring; 9.5mm	1095ML7	EUDAMEDFDA UDI	Class IIa	Active
CleanTouch PVA Eye Spears	ML100	EUDAMEDFDA UDI	Class I	Active
Clb®	ML7070 (0)	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP6S0SP-21040P	EUDAMED	Class IIa	Active
ML7 Shipping Case	2000ML7	EUDAMED	Class IIa	Active
ML7 Handpiece	1400ML7	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7100 (-30)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7100 (-10)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7100 (+10)	EUDAMEDFDA UDI	Class IIa	Active
CataPulse Power Cord	1602PC	EUDAMED	Class IIa	Active
CataPulse Console	CP1700	EUDAMED	Class IIb	Active
Clb®	ML7100 (0)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7090 (0)	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP6S0SP-21030S	EUDAMED	Class IIa	Active
Clb®	ML7090 (-20)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7020 (-20)	EUDAMEDFDA UDI	Class IIa	Active
Vacuum Ring; 10.0mm	100ML7	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7030 (+10)	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP530SS-2002PX	EUDAMED	Class IIa	Active
Clb®	ML7030 (-20)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7020 (+10)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7070 (+20)	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP6S0SP-23040S	EUDAMED	Class IIa	Active
Clb®	ML7050 (+20)	EUDAMEDFDA UDI	Class IIa	Active
CleanTouch PVA Eye Spears - Bulk	ML100B	EUDAMED	Class I	Active
CataPulse Cart	CP1900	EUDAMED	Class I	Active
Clb®	ML7030 (-10)	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP414SS-2000LH	EUDAMED	Class IIa	Active
Cannula	CP6S0SS-230400	EUDAMED	Class IIa	Active
Vacuum Ring; 8.5mm	1085ML7	EUDAMEDFDA UDI	Class IIa	Active
CataPulse Shipping Case	CP2000	EUDAMED	Class IIa	Active
Vitrectomy Kit	CP2200	EUDAMED	Class IIa	Active
ML7 Console	1700ML7	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7030 (+20)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7050 (+10)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7071 (-10)	EUDAMED	Class IIa	Active
Cannula	CP5S0SP-2102P0	EUDAMED	Class IIa	Active
ML7 Helical Drive Wrench	1350ML7	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7061 (-10)	EUDAMEDFDA UDI	Class IIa	Active
Clb®	ML7070 (+10)	EUDAMEDFDA UDI	Class IIa	Active
Cannula	CP513SS-1903PH	EUDAMED	Class IIa	Active
ML7 Power Cord	1602PC	EUDAMED	Class IIa	Active
Clb®	ML7050 (0)	EUDAMEDFDA UDI	Class IIa	Active

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FDA Recalls (1)

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

Med Logics Inc. has one FDA recall record initiated on January 13, 2015, which is marked as terminated. The recall pertains to the ML 7090 Calibrated LASIK Blade (CLB), with the reason stated as incompatibility with the AMO Amadeus Metal Blade Holder.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jan 13, 2015	Z-1268-2015	—	terminated	The ML 7090 Calibrated LASIK Blade (CLB) will not fit into the AMO Amadeus Metal Blade Holder.