Seiler Instrument & Mfg. Co., Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1927430
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Low-Power Binocular Loupe Ref K875124
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1927430
- Address
- 3433 Tree Court Industrial Blvd, Saint Louis, MO, 63122
Frequently asked questions
How many devices does Seiler Instrument & Mfg. Co.,Inc. have in the registry?
The registry currently lists 1 device for Seiler Instrument & Mfg. Co.,Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seiler Instrument & Mfg. Co.,Inc.'s devices?
Among its 1 most recently registered device, Seiler Instrument & Mfg. Co.,Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Seiler Instrument & Mfg. Co.,Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Seiler Instrument & Mfg. Co.,Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Seiler Instrument & Mfg. Co.,Inc. in the registry?
The most recently registered devices listed for Seiler Instrument & Mfg. Co.,Inc. include LOW-POWER BINOCULAR LOUPE.