Med Logics Inc
Active in EUDAMEDUnited Statesfrom SRN EUDAMED SRN US-MF-000004600
Med Logics Inc is a medical device manufacturer based in the United States, with 130 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (EU Class IIa and I; FDA Class I and II) and 1 FDA recall as of 14 Nov 2026.
- Devices
- 130
- Registrations
- EUDAMED
- FDA recalls
- 1
Registry facts
- Registries
- EUDAMED 114
- FDA GUDID 60
- FDA 510(k) 12
- Device classes
- EU Class IIa 107
- FDA Class I 13
- EU Class I 5
- FDA Class II 3
- EU Class IIb 2
- Top EMDN categories
- FDA recalls
- Sites and related companies
- E C Rep Limited authorised representative
- Identifiers
- EUDAMED SRN US-MF-000004600
- DUNS 075390489
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA recalls
- Authorised rep.
- E C Rep LimitedIE
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.
Catalogue
Search and filter all 130 devicesShowing 1-50 of 130
Company details
- EUDAMED SRN
- US-MF-000004600
- DUNS number
- 075390489
- EUDAMED status
- Active
- EUDAMED registered name
- Med-Logics, Inc.
- EUDAMED abbreviated name
- Med-Logics, Inc.
- Registered address
- 1627 Enterprise Street, 75751, Athens, United States
- Website
- www.mlogics.com
- Phone
- 9495823891
- PRRC contact
- Justin Ross
FDA recalls
FDA recall records list 1 recall initiated by MED LOGICS INC, initiated on 2015-01-13. By recorded status: 1 terminated. The reasons filed fall into these groups: performance or accuracy. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2015
- 13 Jan 2015 Z-1268-2015 Class II Terminated The ML 7090 Calibrated LASIK Blade (CLB) will not fit into the AMO Amadeus Metal Blade Holder.
Frequently asked questions
How many devices does MED LOGICS INC have in the registry?
The registry currently lists 130 devices for MED LOGICS INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MED LOGICS INC's devices?
Among its 50 most recently registered devices, MED LOGICS INC has devices listed in EUDAMED (34 devices), FDA 510(k) (12 devices) and FDA GUDID (24 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MED LOGICS INC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for MED LOGICS INC's devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for MED LOGICS INC?
FDA recall records list 1 recall initiated by MED LOGICS INC, the most recent initiated on 13 Jan 2015. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from MED LOGICS INC in the registry?
The most recently registered devices listed for MED LOGICS INC include ML7003, ML7040 (Plus 20) ML7040 (+20), ML7040 (Minus 20) ML7040 (-20) and ML7040 (Plano) ML7040 (0).