Glove Seal Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 2
What Glove Seal Sdn Bhd makes
Glove Seal Sdn Bhd manufactures latex patient examination gloves, including the standard Patient Examination Glove (Latex) and the Glove Seal D’Pro Latex Examination Glove, designed for medical and clinical use.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway in the United States. The company is based in the US.
Catalogue
Patient Examination Glove (Latex) Ref K891147
Regimes: 510(k) Registry: 510(k)Glove Seal D'pro Latex Examination Glove Ref K983570
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Glove Seal Sdn Bhd have in the registry?
The registry currently lists 2 devices for Glove Seal Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glove Seal Sdn Bhd's devices?
Among its 2 most recently registered devices, Glove Seal Sdn Bhd has devices listed in FDA 510(k) (2 devices).
What risk classes do Glove Seal Sdn Bhd's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Glove Seal Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Glove Seal Sdn Bhd in the registry?
The most recently registered devices listed for Glove Seal Sdn Bhd include PATIENT EXAMINATION GLOVE (LATEX) and GLOVE SEAL D'PRO LATEX EXAMINATION GLOVE.