# K091120: Medpor Contain Implant

- Pathway: 510(k) (Traditional)
- Applicant: Porex Surgical, Inc.
- Decided: Mar 19, 2010 after 336 days
- Product code: NPK (Barrier, Synthetic, Intraoral)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K922627 (1994). 17 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922489: Medpor Surg Implant Material:Prefor Cran/Fac Impla, Porex Technologies Corp. (1992) Summary page 1.
- K051267: Gore Resolut Regenerative Material, Gore Resolut XT Regenerative Membrane, Gore Osseoquest Regenerative Membrane, W. L. Gore & Associates, Inc. (2005) Summary page 1.
- K984230: Osteo-Mesh TM-300, Osteogenics Biomedical, Inc. (1999) Summary page 1.
- K972278: Cytoplast Regentex Titanium 250, Osteogenics Co. (1997) Summary page 1.
- K970841: Imtec/Titanium Mesh, Imtec Corp. (1997) Summary page 1.

## Most influential descendants
- K102184: Medpor Contain Can Implant (2011), 0 descendants of its own

## Indications for use
The MEDPOR CONTAIN Implant is intended to stabilize, support and provide space maintenance for bone graft materials in the maxilla, mandible and zygoma.

Source page: https://510kreport.com/device/K091120
Methodology: https://510kreport.com/methodology