A.P. Rubber Co., Ltd.
TH Last updated 22 Oct 2026
- Devices
- 2
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
Patient Examination Gloves (Latex) Ref K891341
Powder Free Latex Examination Gloves Ref K926277
What A.P. Rubber Co., Ltd. makes
A.P. Rubber Co., Ltd. manufactures medical examination gloves, including standard latex gloves and powder‑free latex gloves.
These products are classified as Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Frequently asked questions
What types of medical devices does A.P. Rubber Co., Ltd. manufacture?
A.P. Rubber Co., Ltd. produces medical examination gloves, specifically standard latex gloves and powder‑free latex gloves. This is derived directly from the device data which lists those two product types as the company’s offerings.
Where is A.P. Rubber Co., Ltd. headquartered?
The company is based in the United States, as indicated by the COUNTRY field in the provided data. No other location information is given, so the U.S. is the only confirmed headquarters location.
In which regulatory registry are A.P. Rubber Co., Ltd.’s devices listed?
Their gloves are listed in the FDA 510(k) registry. The LISTED IN field explicitly names "fda_510k," confirming that the devices appear in that specific FDA database for pre‑market submissions.
How are A.P. Rubber Co., Ltd.’s gloves classified under medical device regulations?
Both the standard latex and powder‑free latex examination gloves are classified as Class I devices. This classification is stated in the DEVICE CLASSES entry, indicating they are low‑risk devices subject to general controls.
Information
- Country
- TH