Trico Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Trico Intl., Inc. makes
Trico Intl., Inc. manufactures single-use EDGE syringes and needles, designed for medical and procedural use, as well as latex examination gloves for healthcare professionals.
The company’s portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Edge Syringes And Needles Ref K923321
Regimes: 510(k) Registry: 510(k)Latex Examination Gloves Ref K923772
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Trico Intl., Inc. have in the registry?
The registry currently lists 2 devices for Trico Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trico Intl., Inc.'s devices?
Among its 2 most recently registered devices, Trico Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Trico Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Trico Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trico Intl., Inc. in the registry?
The most recently registered devices listed for Trico Intl., Inc. include EDGE SYRINGES AND NEEDLES and LATEX EXAMINATION GLOVES.