Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LANDERS THREE STRUT VITRECTOMY LENS RING

K-Number: K912151 · 1991-07-25

ApplicantOcular Instruments, Inc.
Decision Date1991-07-25
Product CodeHNH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LANDERS THREE STRUT VITRECTOMY LENS RING is the device name listed in this FDA 510(k) record. The listed applicant is Ocular Instruments, Inc.. It received FDA 510(k) clearance on 1991-07-25 under 510(k) number K912151. The device is classified under product code HNH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANDERS THREE STRUT VITRECTOMY LENS RING?

LANDERS THREE STRUT VITRECTOMY LENS RING is a medical device that received FDA 510(k) clearance on 1991-07-25. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K912151.

When did LANDERS THREE STRUT VITRECTOMY LENS RING receive FDA 510(k) clearance?

LANDERS THREE STRUT VITRECTOMY LENS RING received FDA 510(k) clearance on 1991-07-25, under 510(k) number K912151.

Who is the listed applicant for LANDERS THREE STRUT VITRECTOMY LENS RING?

The FDA 510(k) record lists Ocular Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LANDERS THREE STRUT VITRECTOMY LENS RING?

The FDA product code for LANDERS THREE STRUT VITRECTOMY LENS RING is HNH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ocular Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K014170STAURENGHI WIDE FIELD SCANNING LASER LENSK012096DISPOSABLE VITRECTOMY LENSK933976MANDELKORN SUTURE LYSIS LENSK933264RITCH NYLON SUTURE LASER LENSK94142050 DEGREE HRI PRISM LENSK935302OSHER SURGICAL GONIO/POSTERIOR POLE LENS

View all 50 devices →

Related Devices (Code: HNH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K912269LANDERS NOTCHED IRRIGATING VITRECTOMY LENS RINGOcular Instruments, Inc.K912268LANDERS NOTCHED VITRECTOMY LENS RINGOcular Instruments, Inc.K902496LANDERS VITRECTOMY LENS RING W/INFUSIONOcular Instruments, Inc.K863775RK VACUUM FIXATION RING SYSTEMAmeritek, Inc.K850991LANDERS VITRECTOMY LENS RING SYSTEMSOcular Instruments, Inc.K832912GELENDER VACUUM FIXATION RING SYSMiami Eye Technology, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑