Pepin Mfg., Inc.
United StatesFDA applicant, unverified FDA FEI 1000221051
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Comfort/Io Iontophoresis Electrodes Ref K060579
Regimes: 510(k) Registry: 510(k)Pmi Tens Electrode Ref K932849
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000221051
- Address
- 1875 HWY 61 SOUTH, LAKE CITY, MN, 55041
Frequently asked questions
How many devices does Pepin Mfg., Inc. have in the registry?
The registry currently lists 3 devices for Pepin Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pepin Mfg., Inc.'s devices?
Among its 3 most recently registered devices, Pepin Mfg., Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Pepin Mfg., Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pepin Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pepin Mfg., Inc. in the registry?
The most recently registered devices listed for Pepin Mfg., Inc. include CUTANEOUS ELECTROTHERAPY AND RECORDING ELECTRODES; TENS ELECTRODES, COMFORT/IO IONTOPHORESIS ELECTRODES and PMI TENS ELECTRODE.