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Shinhung MST Co., Ltd. · Model STW4510LS · UDI-DI 08809457204861
1
510(k) clearances
0
Adverse events
211
Recalls
327
Facilities
Description
The Stella is intended to be surgically placed in the upper or lower jawbone to provide support for prosthetic devices, such as artificial teeth, restoring the patient's chewing capabilities. The Stella is intended for delayed loading and immediate loading is possible when good primary stability is achieved and with appropriate occlusal loading. The Stella Abutment is intended to be connected to the dental implant to retain the overdenture or partial denture.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-16 | Straumann USA LLC | Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest |
| 2025-07-30 | S.I.N. Implant System Ltda | Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which |
| 2025-05-01 | Straumann USA LLC | It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead. |
| 2025-05-01 | Straumann USA LLC | It is possible that a package labelled as an 11.5 mm implant may contain a 13 mm implant instead. |
| 2025-01-10 | Nobel Biocare | Due to manufacturing issue (unintended by-product of the injection molding process) a sharp pin that may puncture the blister packaging and breaching the sterile barrier of the fin |
| 2024-09-01 | SIN SISTEMA DE IMPLANTE NACIONAL S.A | Dental implant box incorrectly labels the diameter as 4,5 X 18,0 mm, but the internal label correctly labels the diameter as 4,0 X 18,0 mm; if the dentist drills the bone with the |
| 2023-04-06 | Hiossen Inc. | Mis-labeled length of the dental implant on the Recall Implant's package. Dental implant size D5.0 x L8.5mm, labeled as D5.0 x L10mm |
| 2022-07-25 | Nobel Biocare | Due to the presence of a burr which may cause an aspiration risk to patient during surgical procedure. |
| 2021-12-17 | Nobel Biocare Usa Llc | Due to 16 complaints related to drivers not engaging in implants. According to the firm's investigations, the incorrect offset gauge was potentially used during production of the |
| 2021-11-30 | Straumann USA LLC | Mislabeled: Carton box item 138.089- Easypack Helix GM Acqua 3.5X8/Smart 4.5X2.5 has an implant with measure of 3.5x13mm; and Carton Box (138.107- Easypack Helix GM Acqua has a 3.5 |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
