Precision Therapeutics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Precision Therapeutics, Inc. makes
Precision Therapeutics, Inc. manufactures a tapeless eye shield designed for post-operative care and a lid splint used to immobilize the eyelid during healing.
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
Tapeless Eye Shield Ref K872659
510(k) 510(k)Lidsplint Ref K864810
510(k) 510(k)
Frequently asked questions
How many devices does Precision Therapeutics, Inc. have in the registry?
The registry currently lists 2 devices for Precision Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precision Therapeutics, Inc.'s devices?
Among its 2 most recently registered devices, Precision Therapeutics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Precision Therapeutics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Precision Therapeutics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Precision Therapeutics, Inc. in the registry?
The most recently registered devices listed for Precision Therapeutics, Inc. include TAPELESS EYE SHIELD and LIDSPLINT.