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OLV-1-TN Landers Tall Notched Vitrectomy Lens Ring

EUDAMEDFDA UDIFDA 510(k)

Class I (EU MDR)

Ref 5739510(k) K912268

by Ocular Instruments Inc.

Identity

Trade Name
OLV-1-TN Landers Tall Notched Vitrectomy Lens Ring EUDAMED
Landers Tall Notched Vitrectomy Lens Ring FDA UDI
Generic Name
Vitrectomy sutureless lens holding ring, reusable FDA UDI
Device Name
Contact Ophthalmic EUDAMED
Model / Reference
5739 EUDAMED
OLV-1-TN FDA UDI

Identifiers

Primary DI / UDI-DI
00630238057394 EUDAMEDFDA UDI
Basic UDI-DI
06302381262637 EUDAMED
510(k) Number
K912151 FDA UDI
FDA Product Code
HNH FDA UDI
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
GMDN Term
Vitrectomy sutureless lens holding ring, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.4350 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

OLV-1-TN Landers Tall Notched Vitrectomy Lens Ring by Ocular Instruments, Inc. — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k)

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000007216
FDA Applicant
Ocular Instruments, Inc.
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (3)

  • EUDAMED c7227581-36c9-4b0a-b037-e98a3116092a 85 fields · synced Jun 18, 2026
  • FDA UDI 15e5469b-8db2-4965-ade6-6caed2f6c31d 33 fields · synced May 30, 2026
  • FDA 510(k) K912268 1 fields · synced May 18, 2026