# K262983: EsTemp Implant

- Pathway: 510(k) (Special)
- Applicant: Spident Co., Ltd.
- Decided: Sep 25, 2026 after 29 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K033309 (2004). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K134021: Estemp Implant, Estemp Clear, Spident Co., Ltd. (2014) Summary page 5.

## Indications for use
- For temporary cementation of provisional restorations attached to implant abutments. - For temporary retention and retrievable cementation of implant-supported restorations.

Source page: https://510kreport.com/device/K262983
Methodology: https://510kreport.com/methodology