Suppliers / Dental Technologies

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.

0
active US DMFs
0
valid CEPs
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
Plants
1 of 1 confirmed
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

Questions about Dental Technologies

Does Dental Technologies hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Dental Technologies. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Dental Technologies FDA-registered?
One site operated by Dental Technologies carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Dental Technologies's last inspection go?
The most recent inspection on record closed on 14 August 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file, of which 3 closed as OAI.
Where does Dental Technologies manufacture?
2 registered sites are on record, in Portugal and United States (Porto and Lincolnwood). Every site is listed on this page with the register it came from.
Which regulators recognise Dental Technologies's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 14 August 2024.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates