Aaron Medical Industries
Country not established
- Devices
- 46
- FDA recalls
- 2
At a glance
Market reach
- United States
- FDA recalls
What Aaron Medical Industries makes
Aaron Medical Industries manufactures electrosurgical devices for cutting, coagulation, and tissue management, including hand controls, electrodes, generators, and accessories. Their portfolio includes disposable and reusable tools like the ElectroSurge HandControl Pencil, Laparoscopic Electrodes, and high-frequency generators such as the A1250 and A900. Additional products cover cautery tools (low and high temperature), a suture remover system, and specialized accessories like a third-hand helper for surgical precision.
The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) registry, reflecting their regulatory compliance. The manufacturer operates from the United States.
Catalogue
Search and filter all 46 devicesFDA recalls
FDA recall records list 2 recalls initiated by Aaron Medical Industries, initiated on 2004-06-29. By recorded status: 2 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2004
- 29 Jun 2004 Z-1238-04 Unclassified (pre-2012) Terminated The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.
Full distribution text
- 29 Jun 2004 Z-1239-04 Unclassified (pre-2012) Terminated The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.
Full distribution text
- 29 Jun 2004 Z-1238-04 Unclassified (pre-2012) Terminated The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.
Frequently asked questions
How many devices does Aaron Medical Industries have in the registry?
The registry currently lists 46 devices for Aaron Medical Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aaron Medical Industries's devices?
Among its 46 most recently registered devices, Aaron Medical Industries has devices listed in FDA 510(k) (46 devices).
What risk classes do Aaron Medical Industries's devices fall under?
Among its 46 most recently registered devices, the classes recorded for Aaron Medical Industries's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Aaron Medical Industries?
FDA recall records list 2 recalls initiated by Aaron Medical Industries, the most recent initiated on 29 Jun 2004. 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 Aaron Medical Industries in the registry?
The most recently registered devices listed for Aaron Medical Industries include AARON ELECTROSURGICAL HANDCONTROL PENCIL, MODEL ESP5, RESISTICK SOLID LAPAROSCOPIC ELECTRODES, NEURO PULSE II, III and DEVICE, ELECTROSURGICAL, CUTTING AND COAGULATION & ACCESSORIES.