Dental Technologies
United States 38 employees Updated 9 July 2026
Dental Technologies is a finished-dose manufacturer based in United States. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 14 August 2024 as VAI.
2
registered plants
1 with an FDA FEI number
1
filings
across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.
Inspection history
- 14 August 2024 VAI US FDA
- 26 July 2022 OAI US FDA
- 20 January 2021 OAI US FDA
- 12 March 2019 VAI US FDA
- 29 June 2017 NAI US FDA
- 9 January 2015 NAI US FDA
- 23 March 2012 VAI US FDA
- 12 April 2011 OAI US FDA
NAI means no action indicated, VAI means voluntary action indicated, and OAI means
official action indicated.
Registered plants
| Site | FDA FEI |
| Porto, Portugal | Not on file |
| LINCOLNWOOD, United States | 1413475 |
Filings and GMP by regulator
| Regulator | Filings | GMP certificates |
| NPRA (MY) | 1 | None |
| US FDA | None | 1 |
Comparing suppliers?
Choose your molecules and target markets. Dental Technologies comes back tiered against every other
supplier able to file there.
Start for free No sales call.
Open risk flags
- The most recent inspection outcome was VAI, on 14 August 2024.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates