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FDA 510(k)

SYNERGEYES PS HYBRID CONTACT LENS

K-Number: K060102 · 2006-03-15

ApplicantSynergeyes, Inc.
Decision Date2006-03-15
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SYNERGEYES PS HYBRID CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Synergeyes, Inc.. It received FDA 510(k) clearance on 2006-03-15 under 510(k) number K060102. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNERGEYES PS HYBRID CONTACT LENS?

SYNERGEYES PS HYBRID CONTACT LENS is a medical device that received FDA 510(k) clearance on 2006-03-15. The listed applicant is Synergeyes, Inc.. The 510(k) number is K060102.

When did SYNERGEYES PS HYBRID CONTACT LENS receive FDA 510(k) clearance?

SYNERGEYES PS HYBRID CONTACT LENS received FDA 510(k) clearance on 2006-03-15, under 510(k) number K060102.

Who is the listed applicant for SYNERGEYES PS HYBRID CONTACT LENS?

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

What is the FDA product code for SYNERGEYES PS HYBRID CONTACT LENS?

The FDA product code for SYNERGEYES PS HYBRID CONTACT LENS is HQD.

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Other records listing Synergeyes, 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.

K153714SynergEyes A&M (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes KC (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes PS (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes SiH (petrafocon A hem-larafilcon A) Hybrid Daily Wear Contact Lens, SynergEyes UltraHealth for Keratoconus (petrafocon A hem-larafilcon A) Hybrid Daily Wear CoK160938SynergEyes SiH with Hydra-PEG(petrafocon A hem-larafilcon A) Hybrid Daily Wear LensK113586SYNERGEYES SIH (PETRAFOCON A HEM-LARAFILCON A) HYBRID CONTACT LENSK083921SYNERGEYES SIG (PETRAFOCON A HEM-LARAFILCON A) HYBRID CONTACT LENSK081034SYNERGEYES HYBRID CONTACT LENSES - DAILY WEAR, MODELS A, M, KC AND PSK080193SYNERGEYES HYBRID CONTACT LENSES-DAILY WEAR

View all 8 devices →

Related Devices (Code: HQD)

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.

K253822GPA (hexafocon A) Rigid Gas Permeable Contact LensesZhuhai Fitlens Medical Technology Co., Ltd.K242393Acuity 181™ (tisilfocon A) and Acuity 181™ (tisilfocon A) with Tangible™ Hydra-PEG® Rigid Gas Permeable Contact LensesAcuity Polymers, Inc.K241398SDJMASTERVISION (fluoroxyfocon A) Rigid Gas Permeable Contact LensesTianjin Mastervision Technology Co., Ltd.K241571BostonSight® Specialty LensesBoston Foundation For Sight, Inc. D/B/A BostonsightK240618Acuity 200™ (fluoroxyfocon A) Rigid Gas Permeable Contact Lens; Acuity 100™ (hexafocon A) Rigid Gas Permeable Contact Lens; Acuity 200™ with Tangible® Hydra-PEG® (fluoroxyfocon A) Rigid Gas Permeable Contact Lens; Acuity 100™ with Tangible® Hydra-PEG® (hexafocon A) Rigid Gas Permeable Contact LensAcuity Polymers, Inc.K233325Visionary Optics Scleral Contact Lens (roflufocon D, roflufocon E, hexafocon A, hexafocon B, tisilfocon A, fluoroxyfocon A)Visionary Optics, LLC

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.

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