Not currently registered with FDA under this name
Philips Electronics UK Limited
Houston, TX, United States. Named as applicant on 1 dental 510(k) clearance between 2009 and 2009. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 12009–2009
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Philips Electronics UK Limited as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 18 Jun 2009 | K090167 | PHILIPS AVENT CLASSIC STAGE 2 AND 3 TEETHER, MODEL SCF882/01, SCF884/01, PHILIPS AVENT ANIMAL STAGE 2 AND 3 TEETHER, | KKO Fluid-Filled Teething Ring |
Some of these clearances are listed with FDA today by another company: Fitson Sdn Bhd (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.