# K002886: Implantech Composite Facial Implants (Malar, Chin, and Nasal)

- Pathway: 510(k) (Traditional)
- Applicant: Implantech Associates, Inc.
- Decided: Nov 24, 2000 after 70 days
- Product code: LZK (Implant, Malar)
- Device class: 2
- Regulation: 21 CFR 878.3550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K091011: Pureform Eptfe Facial Implants (Nasal, Chin, Maler) (2009), 1 descendant of its own
- K201153: Tisuthes e-PTFE Surgical Patch (2023), 0 descendants of its own
- K172389: ePTFE-Coated Auricular Implant (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K002886
Methodology: https://510kreport.com/methodology