Scopix LTD
IsraelFDA applicant, unverified FDA FEI 3044828322
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Scopix LTD makes
Scopix, Ltd. manufactures the TL-10 Laparoscopic Scope Cleaner, a device designed for the cleaning and maintenance of laparoscopic scopes to ensure proper sterilization and reuse in surgical procedures.
The TL-10 Laparoscopic Scope Cleaner is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
TL-10 Laparoscopic Scope Cleaner Ref K260089
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3044828322
- DUNS number
- 521149674
- Address
- 108 Kalanit St, Amikam Northern
Frequently asked questions
How many devices does Scopix LTD have in the registry?
The registry currently lists 2 devices for Scopix LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scopix LTD's devices?
Among its 2 most recently registered devices, Scopix LTD has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Scopix LTD's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Scopix LTD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scopix LTD in the registry?
The most recently registered devices listed for Scopix LTD include TL10 and TL-10 Laparoscopic Scope Cleaner.