Medpor Ocular Peg System and Accessories

by Porex Technologies Corp. of Georgia 510(k)

Active United States

510(k) K960859

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK960859	Date29 May 1996Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 12 Oct 2026.

Specification

510(k)

510(k) Number: K960859
FDA Product Code: HPZ

Device Class: Class II
Regulation: 21 CFR Part 886.3320
Advisory Committee: Ophthalmic
FDA Decision: SESE Substantially Equivalent

Other devices from Porex Technologies Corp. of Georgia

Ossicular Prosthesis: 8 Partial, 3 Total

Class II