PMA approvals

TECNIS Foldable Acrylic IOL with OptiEdge, Model ZA9003

Johnson & Johnson Surgical Vision, Inc. · intraocular lens · Ophthalmic

P990080 S067SupplementOK30
Open FDA's page for this record
PMA number
P990080
Supplement number
S067
Applicant
Johnson & Johnson Surgical Vision, Inc.
Street 1
31 Technology Dr., Suite 200
City
Irvine
State
CA
Zip
92618
Generic name
intraocular lens
Trade name
TECNIS Foldable Acrylic IOL with OptiEdge, Model ZA9003
Product code
HQL
Advisory committee
OP
Advisory committee description
Ophthalmic
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited review flag
N
Date received
2026-09-21
Decision date
2026-10-19
Decision code
OK30
Ao statement

the transfer of microbiology testing from an external contractor to an in-house laboratory to support product manufacturing at the AMO Puerto Rico manufacturing site

Harmonized identifiers (openFDA)
Device name
Intraocular Lens
Medical specialty description
Ophthalmic
Regulation number
886.3600
Device class
3
Registration number
9613160, 1038833, 3013202565, 3015456951, 3010155661, 2030624, 1048735, 3017435679, 3014002883, 9681121, 1119421, 9612169, 2648035, 3010413216, 1054811, 3014173684, 3008344633, 3006723646, 3012304651, 2438659, 2023826, 3010126268, 3007207818, 3006946276, 1281950, 9710098, 3003304724, 3024715547, 2032098, 1610287, 2031928, 2031959, 1119279, 2011171, 9614546, 3017636737, 1037089, 9614429, 9681630, 3008449456 +17 more
FEI number
1038833, 3013202565, 3001659659, 3015456951, 3001284430, 3010155661, 1048735, 3017435679, 1000121259, 3014002883, 1119421, 2648035, 3010413216, 3014173684, 3008344633, 3002936283, 3002777043, 3006723646, 3012304651, 3004651700, 2023826, 3010126268, 3007207818, 3006946276, 1281950, 3003088462, 3003304724, 3002023310, 3024715547, 1000306431, 3002807944, 1610287, 1119279, 2011171, 3017636737, 1037089, 3003058448, 1317628, 3002808262, 3002808259 +17 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.