FDA PMA FDA Class 3 Approved 🇺🇸 United States

Lens, Contact, Orthokeratology, Overnight

PMA: P040029 · Supplement: S006 · Decision Aug 7, 2019
Classifications
1
FEI Numbers
14
Registration Numbers
14

Basic Information

Device Name
Lens, Contact, Orthokeratology, Overnight
Trade Name
Euclid Systems Orthokeratology (oprifoconA)/ Contact Lenses for Overnight Wear/Euclid Systems Orthokeratology (tisilfoco
PMA Number
P040029
Supplement Number
S006
Device Class
FDA Class 3
Product Code
NUU
Generic Name
Lens, contact, orthokeratology, overnight
Regulation Number
886.5916
Medical Specialty
Ophthalmic
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
August 7, 2019
Date Received
September 29, 2017
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for new manufacturing site at Euclid Systems Corporation, 45472 Holiday Drive, Suite 7, Sterling, VA.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NUU Lens, Contact, Orthokeratology, Overnight