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Sign in to claim this brandMED 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
- —
- —
- [email protected]
- Phone
- 9495823891
- PRRC Contact
- Justin Ross
- EUDAMED SRN
- US-MF-000004600
- FDA FEI Number
- —
- DUNS Number
- 075390489
Catalogue (106)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ml7003 | ML7003 | FDA UDI | Class I | Active |
| ML7040 (Plus 20) | ML7040 (+20) | FDA UDI | Class I | Active |
| ML7040 (Minus 20) | ML7040 (-20) | FDA UDI | Class I | Active |
| ML7040 (Plano) | ML7040 (0) | FDA UDI | Class I | Active |
| Clb® | ML7070 (-10) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7020 (-10) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7061 (+10) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7050 (-20) | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula | CP416SP-2000LH | EUDAMED | Class IIa | Active |
| Cannula | CP6S0SS-230300 | EUDAMED | Class IIa | Active |
| Clb® | ML7020 (+20) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7061 (+20) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7050 (-30) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7020 (0) | EUDAMEDFDA UDI | Class IIa | Active |
| Vacuum Tubing | ML8001VS | EUDAMEDFDA UDI | Class I | Active |
| Cannula | CP6S0SP-21040S | EUDAMED | Class IIa | Active |
| Clb® | ML7050 (-10) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7100 (+20) | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula | CP414SP-1900LH | EUDAMED | Class IIa | Active |
| Clb® | ML7070 (-20) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7061 (0) | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7071 (+20) | EUDAMED | Class IIa | Active |
| Vacuum Ring; 8.0mm | 1080ML7 | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula | CP416SP-1900LH | EUDAMED | Class IIa | Active |
| Clb® | ML7070 (-30) | EUDAMEDFDA UDI | Class IIa | Active |
| ML7 Head; 130µm | 0130ML7 | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7061 (-20) | EUDAMEDFDA UDI | Class IIa | Active |
| Vacuum Tubing | ML8060VS | EUDAMEDFDA UDI | Class I | Active |
| Ml Microkeratome Blade | K962661 | FDA 510(k) | Class I | Active |
| Med-Logics Microkeratome Blade, Model 7020clb | K022716 | FDA 510(k) | Class I | Active |
| Ml Eye Spear, Model Ml 27 Es | K002279 | FDA 510(k) | Class II | Active |
| Medlogics Ml 4000, Model 4000 | K002515 | FDA 510(k) | Class I | Active |
| Med-Logics Disposable Alk Tubing | K010353 | FDA 510(k) | Class I | Active |
| Med-Logics, Model Ml7090 | K033293 | FDA 510(k) | Class I | Active |
| Med-Logics Microkeratome Blade, Model 7050clb | K022982 | FDA 510(k) | Class I | Active |
| Ml Universal Tubing | K983448 | FDA 510(k) | Class II | Active |
| Ml Microkeratome | K981071 | FDA 510(k) | Class I | Active |
| Ml Blade, Model Ml7030 | K010872 | FDA 510(k) | Class I | Active |
| Ml-Disposable Pak | K972522 | FDA 510(k) | Class II | Active |
| Ml Disposable Alk Tubing | K971173 | FDA 510(k) | Class I | Active |
| Clb® | ML7090 (+20) | EUDAMEDFDA UDI | Class IIa | Active |
| ML7 Cart | 1900ML7 | EUDAMED | Class IIa | Active |
| Clb® | ML7030 (0) | EUDAMEDFDA UDI | Class IIa | Active |
| Titanium Eye Marker | 2100ML7 | EUDAMEDFDA UDI | Class IIa | Active |
| Clb® | ML7071 (-30) | EUDAMED | Class IIa | Active |
| Clb® | ML7020 (-30) | EUDAMEDFDA UDI | Class IIa | Active |
| Lens Removal Kit | CP2100 | EUDAMED | Class IIa | Active |
| Clb® | ML7061 (-30) | EUDAMEDFDA UDI | Class IIa | Active |
| Cannula | CPC03SP-1900LH | EUDAMED | Class IIa | Active |
| Cannula | CPC02SP-2000LH | EUDAMED | 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. |