Not currently registered with FDA under this name
Pennwalt Corp.
Mchenry, IL, United States. Named as applicant on 5 dental 510(k) clearances between 1980 and 1983. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51980–1983
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names Pennwalt Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 28 Oct 1983 | K833241 | INTREX | EAP Intraoral X-Ray Unit |
| 10 Oct 1980 | K801860 | S.S. WHITE-PENNWALT RENEW CALCIUM HYDROX | EJK Calcium Hydroxide Cavity Liner |
| 9 Jun 1980 | K801274 | S.S. WHITE-PENNWALT PRELUDE PIT SEALANT | EBC Pit and Fissure Sealant and Conditioner |
| 3 Mar 1980 | K800133 | PANOREX II DENTAL X-RAY UNIT | EHD Extraoral with Timer X-Ray Unit |
| 3 Mar 1980 | K800063 | XR-710 | EAP Intraoral X-Ray Unit |
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.