Adler Instrument Company
Also registered as Adler Instrument Co.
Country not established FDA establishment FEI 3010034765
- Devices
- 8
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Container System Ref K831068
510(k) 510(k)Adler Steam Indicator-Gas Indicator Ref K833264
510(k) 510(k)Maxi-Flow Suction Set W/Y Connector Ref K910171
510(k) 510(k)Adler Disposable Bipolar Cord Ref K900913
510(k) 510(k)Maxi-Flow Insufflator Tubing Set Ref K903208
510(k) 510(k)Adler Custom Procedure Packs Ref K841723
510(k) 510(k)Maxi-Flow Insufflator Tubing Set W/Filter Ref K903209
510(k) 510(k)Maxi-Flow Suction Set 12 Ft. Ref K910170
510(k) 510(k)
Company details
- FDA FEI number
- 3010034765
- Address
- 16460 Cortez Blvd, Brooksville, FL, 34601
Frequently asked questions
How many devices does ADLER INSTRUMENT COMPANY have in the registry?
The registry currently lists 8 devices for ADLER INSTRUMENT COMPANY. Devices recorded under merged duplicate company entries are counted once.
Which registries list ADLER INSTRUMENT COMPANY's devices?
Among its 8 most recently registered devices, ADLER INSTRUMENT COMPANY has devices listed in FDA 510(k) (8 devices).
What risk classes do ADLER INSTRUMENT COMPANY's devices fall under?
Among its 8 most recently registered devices, the classes recorded for ADLER INSTRUMENT COMPANY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ADLER INSTRUMENT COMPANY in the registry?
The most recently registered devices listed for ADLER INSTRUMENT COMPANY include CONTAINER SYSTEM, ADLER STEAM INDICATOR-GAS INDICATOR, MAXI-FLOW SUCTION SET W/Y CONNECTOR and ADLER DISPOSABLE BIPOLAR CORD.