Glaxosmithkline Consumer Healthcare
Country not established
- Devices
- 7
What Glaxosmithkline Consumer Healthcare makes
The company manufactures N95 respirators, including flat-fold and double-strap variants, designed for particulate filtration and respiratory protection.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Actiprotect Uc N95 Respirator Ref K093189
Regimes: 510(k) Registry: 510(k)Biotene Oral Balance Gel, Biotene Dry Mouth Oral Rinse, Biotene Moisturizing Mouth Spray Ref K123731
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Actiprotect Uf N95 Respirator Ref K093161
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Glaxosmithkline Consumer Healthcare have in the registry?
The registry currently lists 7 devices for Glaxosmithkline Consumer Healthcare. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glaxosmithkline Consumer Healthcare's devices?
Among its 7 most recently registered devices, Glaxosmithkline Consumer Healthcare has devices listed in FDA 510(k) (7 devices).
What risk classes do Glaxosmithkline Consumer Healthcare's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Glaxosmithkline Consumer Healthcare's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Glaxosmithkline Consumer Healthcare in the registry?
The most recently registered devices listed for Glaxosmithkline Consumer Healthcare include BIOTENE MOISTURIZING MOUTH SPRAY FOR DRY MOUTH SYMPTOM RELIEF, ACTIPROTECT UC N95 RESPIRATOR, BIOTENE ORAL BALANCE GEL, BIOTENE DRY MOUTH ORAL RINSE, BIOTENE MOISTURIZING MOUTH SPRAY and BIOTENE DRY MOUTH MOUTHWASH, BIOTENE PBF DRY MOUTH MOUTHWASH.