# K982753: Seare Biomedical Nasal Implants

- Pathway: 510(k) (Traditional)
- Applicant: Seare Biomedical Corp.
- Decided: Sep 30, 1998 after 55 days
- Product code: FZE (Prosthesis, Nose, Internal)
- Device class: 2
- Regulation: 21 CFR 878.3680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Allied Biomedical Nasal Implants: named in the summary without a submission number

## Indications for use
Seare Biomedical Nasal Implants are intended for use in augmentation and reconstruction of the nasal contour during rhinoplasty. They are intended for insertion via an intraoral or nasal sill incision.

Source page: https://510kreport.com/device/K982753
Methodology: https://510kreport.com/methodology