Physician Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Physician Industries, Inc. makes
Physician Industries, Inc. manufactures single-use medical devices including general hygiene kits for procedural preparation, Durameter syringes for fluid administration, and general procedure kits for surgical and diagnostic use. The company also produces radiofrequency ablation needles designed for controlled tissue treatment procedures.
The portfolio includes Class I and Class II devices, with some products authorised via the FDA’s 510(k) pathway. These devices are listed under U.S. regulatory frameworks, and the company operates from the United States.
Catalogue
General Hygiene Kit Ref K954068
Regimes: 510(k) Registry: 510(k)Physician Industries' Durameter Syringe Ref K033739
Regimes: 510(k) Registry: 510(k)General Procedure Kit Ref K960248
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Physician Industries, Inc. have in the registry?
The registry currently lists 4 devices for Physician Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Physician Industries, Inc.'s devices?
Among its 4 most recently registered devices, Physician Industries, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Physician Industries, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Physician Industries, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Physician Industries, Inc. in the registry?
The most recently registered devices listed for Physician Industries, Inc. include GENERAL HYGIENE KIT, PHYSICIAN INDUSTRIES' DURAMETER SYRINGE, GENERAL PROCEDURE KIT and PHYSICIAN INDUSTRIES RADIOFREQUENCY ABLATION NEEDLE.