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)

SLIT LAMP SL-D4 (Type: LED)

K-Number: K262637 · 2026-09-18

ApplicantTopcon Corporation
Decision Date2026-09-18
Product CodeHJO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SLIT LAMP SL-D4 (Type: LED) is the device name listed in this FDA 510(k) record. The listed applicant is Topcon Corporation. It received FDA 510(k) clearance on 2026-09-18 under 510(k) number K262637. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIT LAMP SL-D4 (Type: LED)?

SLIT LAMP SL-D4 (Type: LED) is a medical device that received FDA 510(k) clearance on 2026-09-18. The listed applicant is Topcon Corporation. The 510(k) number is K262637.

When did SLIT LAMP SL-D4 (Type: LED) receive FDA 510(k) clearance?

SLIT LAMP SL-D4 (Type: LED) received FDA 510(k) clearance on 2026-09-18, under 510(k) number K262637.

Who is the listed applicant for SLIT LAMP SL-D4 (Type: LED)?

The FDA 510(k) record lists Topcon Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLIT LAMP SL-D4 (Type: LED)?

The FDA product code for SLIT LAMP SL-D4 (Type: LED) is HJO.

Other records listing Topcon Corporation 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.

K253039AUTO KERATO-REFRACTO TONOMETER TRK-3 OMNIAK2410813D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1 (type: Maestro2); IMAGEnet6 Ophthalmic Data SystemK2335613D Optical Coherence Tomography (3D OCT-1(type: Maestro2))K232828IMAGEnet6 Ophthalmic Data SystemK2312223D OPTICAL COHERENCE TOMOGRAPHY 3D OCT-1(type: Maestro2)K221111Non-Mydriatic Retinal Camera NW500

View all 12 devices →

Related Devices (Code: HJO)

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.

K253834VISUREF 600Carl Zeiss Vision GmbHK231760HP-OCT (HP-OCT)Cylite Pty. , Ltd.K222372Kowa SL-19Kowa Company , Ltd.K193188MiiS Horus Eye Anterior CameraMedimaging Integrated Solution, Inc (Miis)K182306Sunkingdom Slit LampChongqing Sunkingdom Medical Instrument Co., Ltd.K173771IOLMaster 700Carl Zeiss Meditec, AG

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.

↑