Reliance Medical Products, Inc.
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Reliance Medical Products, Inc. makes
Reliance Medical Products, Inc. manufactures the RELIANCE® 6200 Examination Chair, a medical device designed for patient examinations in clinical settings.
The company’s portfolio is regulated under FDA’s Class I device classification, with the RELIANCE® 6200 Examination Chair listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Reliance(R) 6200 Examination Chair Ref K894018
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 1 recall initiated by Reliance Medical Products, Inc., initiated on 2017-12-06. By recorded status: 1 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.
Recalls initiated per year
- 2017 1
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2017
- 6 Dec 2017 Z-1318-2018 Class II Terminated Product has been found with a missing Washer, Retaining Ring, and/or Stop Screw. Recalling firm was notified by distributor that Refractor Suspension Arm fell on a patient s lower torso along with the arm housing
Full distribution text
- 6 Dec 2017 Z-1318-2018 Class II Terminated Product has been found with a missing Washer, Retaining Ring, and/or Stop Screw. Recalling firm was notified by distributor that Refractor Suspension Arm fell on a patient s lower torso along with the arm housing
Frequently asked questions
How many devices does Reliance Medical Products, Inc. have in the registry?
The registry currently lists 1 device for Reliance Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reliance Medical Products, Inc.'s devices?
Among its 1 most recently registered device, Reliance Medical Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Reliance Medical Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Reliance Medical Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for Reliance Medical Products, Inc.?
FDA recall records list 1 recall initiated by Reliance Medical Products, Inc., the most recent initiated on 6 Dec 2017. 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 Reliance Medical Products, Inc. in the registry?
The most recently registered devices listed for Reliance Medical Products, Inc. include RELIANCE(R) 6200 EXAMINATION CHAIR.