Artiglass SRL
ItalyFDA applicant, unverified FDA FEI 3011744364
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Artiglass SRL makes
Artiglass Srl manufactures glass syringes designed for use in operating rooms, including standard L.O.R. glass syringes and NRFit™ tip variants. These products are intended for single-use medical procedures requiring precise liquid administration or aspiration.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices. These products are listed in the FDA’s 510(k) registry and are based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Artiglass L. O.R. Glass Syringe Ref K122416
Regimes: 510(k) Registry: 510(k)Artiglass NRFitTM Tip L.O.R. Glass Syringes Ref K213800
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011744364
- DUNS number
- 435819227
- Address
- VIA PIEMONTE 13, DUE CARRARE PADOVA
Frequently asked questions
How many devices does Artiglass Srl have in the registry?
The registry currently lists 7 devices for Artiglass Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artiglass Srl's devices?
Among its 7 most recently registered devices, Artiglass Srl has devices listed in FDA 510(k) (2 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Artiglass Srl's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Artiglass Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artiglass Srl in the registry?
The most recently registered devices listed for Artiglass Srl include ARTIGLASS LMC5/LR, ARTIGLASS LLC5/LR, ARTIGLASS LLC10/LR and ARTIGLASS LMC10/LR.