Suredrop, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Suredrop, Inc. makes
Suredrop, Inc. manufactures ocular administration accessories, including an eyedrop guide designed to assist with precise placement of eye drops and an accessory that complements its use.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Accessory To Eyedrop Guide Ref K884974
Regimes: 510(k) Registry: 510(k)Suredrop Eyedrop Guide Ref K874569
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Suredrop, Inc. have in the registry?
The registry currently lists 2 devices for Suredrop, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suredrop, Inc.'s devices?
Among its 2 most recently registered devices, Suredrop, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Suredrop, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Suredrop, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Suredrop, Inc. in the registry?
The most recently registered devices listed for Suredrop, Inc. include ACCESSORY TO EYEDROP GUIDE and SUREDROP EYEDROP GUIDE.