FDA applicant
Jjgc Industria E Comercio DE Materiais Dentarios S.A.
FDA records 40 decisions for Jjgc Industria E Comercio DE Materiais Dentarios S.A. (Curitiba, BR) from 2016 to 2026: 40 510(k) clearances. Most are in product codes DZE (Implant, Endosseous, Root-Form) and NHA (Abutment, Implant, Dental, Endosseous). Since 2016 its 510(k)s took a median of 167 days from receipt to decision, against 187 for FDA’s reviews in the same codes and years. Its devices cite 54 predicates, 33 of them its own earlier devices. 8 recalls are linked to its devices.
FDA’s records also spell it “JJGC Indústria e Comércio de Materiais Dentários S.A.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Jjgc Industria E Comercio DE Materiais Dentarios S.A.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2025
2026 so far, outlined.
Recalls per year
2in 2026
Class I Class II/III not classified
Planning a device like Jjgc Industria E Comercio DE Materiais…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Jjgc”
FDA records each applicant name separately; these may or may not be the same firm.