Porter Instrument Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 6
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Porter Instrument Co., Inc. makes
Porter Instrument Co., Inc. makes automatic vacuum switches, digital flowmeters, clean-air pollution reduction systems, and steam sterilizers including dental autoclaves and automatic steam sterilizers.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Digital Mxr-D Flowmeter Ref K062155
Regimes: 510(k) Registry: 510(k)Clean-Air Pollution Reduction System Ref K802067
Regimes: 510(k) Registry: 510(k)Steam Sterilizer (Autoclave), Dental Ref K895638
Regimes: 510(k) Registry: 510(k)Ses-2012 Automatic Steam Sterilizer Ref K924596
Regimes: 510(k) Registry: 510(k)Mxr-2000 Flowmeter Ref K923781
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 1 recall initiated by Porter Instrument Co., Inc., initiated on 2008-08-26. By recorded status: 1 terminated. The reasons filed fall into these groups: mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2008
- 26 Aug 2008 Z-0228-2009 Unclassified (pre-2012) Terminated inverted check value on the bag tee assembly which can cause leaking of mixed N2O/O2 gas
Frequently asked questions
How many devices does Porter Instrument Co., Inc. have in the registry?
The registry currently lists 6 devices for Porter Instrument Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porter Instrument Co., Inc.'s devices?
Among its 6 most recently registered devices, Porter Instrument Co., Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Porter Instrument Co., Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Porter Instrument Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Porter Instrument Co., Inc.?
FDA recall records list 1 recall initiated by Porter Instrument Co., Inc., the most recent initiated on 26 Aug 2008. 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 Porter Instrument Co., Inc. in the registry?
The most recently registered devices listed for Porter Instrument Co., Inc. include AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000, DIGITAL MXR-D FLOWMETER, CLEAN-AIR POLLUTION REDUCTION SYSTEM and STEAM STERILIZER (AUTOCLAVE), DENTAL.