# K972034: Medpor Ocular Conformer

- Pathway: 510(k) (Traditional)
- Applicant: Porex Surgical, Inc.
- Decided: Jan 20, 1998 after 232 days
- Product code: HQN (Conformer, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.3130
- Recalls of this device: 1 (0 Class I)
- 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) Ophthalmic Conformer marketed by Wilson Ophthalmic Corp.: named in the summary without a submission number

## Recalls of this device
- Mar 28, 2008 · Not classified · Z-2302-2008: The Ocular Conformers were distributed with an expired expiration date.

## Indications for use
The ophthalmic conformer is intended to be used as a post eye surgery device to prevent closure or adhesion during the healing process.

Source page: https://510kreport.com/device/K972034
Methodology: https://510kreport.com/methodology