FDA PMA FDA Class 3 Approved 🇺🇸 United States

Lens, Contact, Orthokeratology, Overnight

PMA: P010062 · Supplement: S008 · Decision Jul 28, 2014
Classifications
1
FEI Numbers
14
Registration Numbers
14

Basic Information

Device Name
Lens, Contact, Orthokeratology, Overnight
Trade Name
BOSTON ORTHOKERATOLOGY (OPRIFOCON A) SHAPING LENS
PMA Number
P010062
Supplement Number
S008
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
July 28, 2014
Date Received
October 20, 2010
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A LABELING UPDATE TO THE PACKAGE INSERT AND PATIENT INFORMATION BOOKLET TO INCLUDE THE RESULTS FROM A SECTION 522 POSTMARKET SURVEILLANCE STUDY (PAS).

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