Cadence Science, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1213649
- Devices
- 63
- Registrations
- FDA
- FDA recalls
- 1
Catalogue
Search and filter all 63 devicesShowing 1-50 of 63
Company details
- FDA FEI number
- 1213649
- Address
- 2080 PLAINFIELD PIKE, Cranston, RI, 02921
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 1
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2019
- 10 May 2019 Z-0365-2020 Class II Terminated The glass syringe used with Pressure Control Syringes may potentially break during use.
Frequently asked questions
How many devices does Cadence Science, Inc. have in the registry?
The registry currently lists 63 devices for Cadence Science, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cadence Science, Inc.'s devices?
Among its 50 most recently registered devices, Cadence Science, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Cadence Science, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Cadence Science, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Cadence Science, Inc.?
FDA recall records list 1 recall initiated by Cadence Science, Inc., the most recent initiated on 10 May 2019. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Cadence Science, Inc. in the registry?
The most recently registered devices listed for Cadence Science, Inc. include Perfektum® 5205, Cadence Science® 5192, MICRO-MATE® 5019 and MICRO-MATE® 5028.