# Saremco Dental AG

- Location (FDA's records): Rebstein, CH
- FDA decisions: 4 (2022–2025): 4 510(k) clearances
- Product codes: EBF (3), KLE (1)
- 510(k) review time since 2016: median 117 days, against 104 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Graphy, Inc.: 1 (https://510kreport.com/company/graphy)
- Dentca, Inc.: 1 (https://510kreport.com/company/dentca)
- Hdi, Inc.: 1 (https://510kreport.com/company/hdi)
- Spident Co., Ltd.: 1 (https://510kreport.com/company/spident)
- 3M Espe AG: 1 (https://510kreport.com/company/3m-espe)

## Firms that cite its devices most
- Vertex-Dental B.V.: 1 (https://510kreport.com/company/vertex-dental)
- Bego Bremer Goldschlägerei Wilh. Herbst GmbH & Co. KG: 1 (https://510kreport.com/company/bego-bremer-goldschlagerei-wilh-herbst)

## Its most-cited devices
- K213343: Saremco Print CROWNTEC (2022), cited by 3

## Recent decisions
- K252151: els unibond (Dec 5, 2025)
- K240823: els extra low shrinkage® composite & els extra low shrinkage® flow (Jun 27, 2024)
- K232050: saremco print BRIDGETEC (Nov 14, 2023)
- K213343: Saremco Print CROWNTEC (Jan 21, 2022)

Source page: https://510kreport.com/company/saremco-dental