Data / Medical devices / Ireland / Aesthetic experts labs ltd
Aesthetic experts labs ltd: FDA-registered device maker in Cork Dublin(County), Ireland, 1 510(k) clearance
Aesthetic experts labs ltd is registered with the FDA (registration 3013576619) in Cork Dublin(County), Ireland. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 10, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013576619
- Address
- 1st Floor 2 Penrose Dock, Victorian Quarter, Cork Dublin(County), Ireland, T23 YY09
- Owner or operator
- Aesthetic expert laboratory (10055014)
- Roles
- Exporter to the US
- First device listed
- May 24, 2017
- Registered through
- 2026
- Brand names listed
- DERMASCULPT, EZCONNECTOR & EZSYRINGE CONNECTOR &EZHOLDER &EZSYRINGE ADAPTOR, EZINJECT, EZSYRINGE; EZSYRINGE BLUE; EZSYRINGE RED; EZSYRINGE WHITE, ezGEL, ezPRF
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Exporter to the US | accessdata.fda.gov |
| Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use | JQC | 1 | Exporter to the US | accessdata.fda.gov |
| Connector, Catheter | GCD | 1 | Exporter to the US | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Exporter to the US | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Exporter to the US | accessdata.fda.gov |
| System, Blood Collection, Vacuum-Assisted, Manual | KST | 1 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 10, 2011 | K103736 | DMC MEDICAL SINGLE-USE POLYCARBONATE SYRINGE | FMF | Substantially Equivalent | Dmc Medical, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Surgical, General & Plastic Surgery
- All makers of System, Blood Collection, Vacuum-Assisted, Manual
- All makers of Syringe, Piston
- All makers of Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use
- All makers of Connector, Catheter
- All makers of Needle, Aspiration And Injection, Disposable
Updated June 10, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.