Rego Latex Progressive Corp.
PH Last updated 22 Oct 2026
- Devices
- 1
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Patient Examination Gloves Ref K894352
What Rego Latex Progressive Corp. makes
Rego Latex Progressive Corp. manufactures patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These devices are classified as Class I under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Frequently asked questions
What types of medical devices does Rego Latex Progressive Corp. manufacture?
Rego Latex Progressive Corp. specializes in manufacturing patient examination gloves, which are single-use medical devices designed to provide barrier protection during procedures. These gloves are intended for use in clinical settings where hygiene and contamination prevention are critical.
Where is Rego Latex Progressive Corp. based?
The company is headquartered in the United States, where it operates as a manufacturer of its listed medical devices.
How are the devices manufactured by Rego Latex Progressive Corp. classified under FDA regulations?
The company’s patient examination gloves fall under Class I classification according to FDA regulations. This classification typically applies to devices posing minimal risk, where general controls are sufficient for ensuring safety and effectiveness.
Are the devices from Rego Latex Progressive Corp. listed in any regulatory registries?
Yes, the company’s devices are documented in the FDA’s 510(k) clearance records, which demonstrate compliance with regulatory requirements for Class I medical devices. This registry confirms that the devices have undergone the necessary pre-market notification process.
Information
- Country
- PH