Profile: Eagle Vision produces silicone punctum plugs, which contain patented Tapered Shaft™ and pivoting wide-flex nose for super retention. We offer products like glaucoma drainage devices, punctum plugs, synthetic dissolvable plugs, schirmer, coroneo punctal gage, graether pupil expander, stents & lid load eyelid weights. Flow controllers may be used when total punctum occlusion is too much. Our tapered shaft is designed to create a vector force, keeping it snugly in the punctal opening where it can be monitored. Our dissolvable punctal/canalicular collagen inserts can be used as a cost-effective way to evaluate the benefits of permanent punctal occlusion.
The company was founded in 1983, has ~30 employees and is ISO, CE certified.
FDA Registration Number: 1034718
50 Products/Services (Click for related suppliers)
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• Audiovisual Training Material |
• Battery-Powered Corneal Burr (FDA Code: HOG / 886.4070) A powered corneal burr is an AC-powered or battery-powered device that is a motor and drilling tool intended to remove rust rings from the cornea of the eye. |
• Castroviejo Double Ended Lacrimal Dilator |
• Collagen Glaucoma Drainage Device |
• Collagen Insert Forceps |
• Collagen Punctum Plugs |
• ColorBarT Schirmer Tear Test |
• CoroneoT Punctal Gage |
• DCR Intubation Stent |
• Disposable Lacrimal Dilators |
• Double Ended Lacrimal Dilator |
• Double Ended Lacrimal Probe |
• ENT Manual Surgical Instrument (FDA Code: LRC / 874.4420) |
• ENT Surgical Tray (FDA Code: MMO / 874.4420) |
• Exophthalmometers (FDA Code: HLS / 886.1270) An exophthalmometer is a device, such as a ruler, gauge, or caliper, intended to measure the degree of exophthalmos (abnormal protrusion of the eyeball). |
• Extended Duration Punctum Plugs |
• Eye Moisture Panels |
• Eye Valve Implant (FDA Code: KYF / 886.3920) An aqueous shunt is an implantable device intended to reduce intraocular pressure in the anterior chamber of the eye in patients with neovascular glaucoma or with glaucoma when medical and conventional surgical treatments have failed. |
• General Surgical Manual Instrument (FDA Code: MDM / 878.4800) A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892. |
• Infant Lacrimal Dilator |
• Iris Retractor Clip (FDA Code: HOC / 886.4350) A manual ophthalmic surgical instrument is a nonpowered, handheld device intended to aid or perform ophthalmic surgical procedures. This generic type of device includes the manual corneal burr, ophthalmic caliper, ophthalmic cannula, eyelid clamp, ophthalmic muscle clamp, iris retractor clip, orbital compressor, ophthalmic curette, cystotome, orbital depressor, lachrymal dilator, erisophake, expressor, ophthalmic forcep, ophthalmic hook, sphere introducer, ophthalmic knife, ophthalmic suturing needle, lachrymal probe, trabeculotomy probe, cornea-sclera punch, ophthalmic retractor, ophthalmic ring (Flieringa), lachrymal sac rongeur, ophthalmic scissors, enucleating snare, ophthalmic spatula, ophthalmic specula, ophthalmic spoon, ophthalmic spud, trabeculotome or ophthalmic manual trephine. |
• Lacrimal Dilator (FDA Code: HNW / 886.4350) |
• Lacrimal Dilators and Cannulas |
• Lacrimal Dilators and Probes |
• Lacrimal Probes (FDA Code: HNL / 886.4350) |
• Lacrimal Punctum Plug |
• Low Power Binocular Loupe (FDA Code: HJH / 886.5120) A low-power binocular loupe is a device that consists of two eyepieces, each with a lens or lens system, intended for medical purposes to magnify the appearance of objects. |
• Measuring Gauge (FDA Code: JYJ / 874.4420) |
• Mini-Lacrimal Probes |
• Monocanalicular Stent |
• Neurosurgical Head Rest (FDA Code: HBM / 882.4440) A neurosurgical headrest is a device used to support the patient's head during a surgical procedure. |
• Ocular Drug Delivery System |
• Ophthalmic Eye Shield (FDA Code: HOY / 886.4750) An ophthalmic eye shield is a device that consists of a plastic or aluminum eye covering intended to protect the eye or retain dressing materials in place. |
• Ophthalmic Eyelid Clamp (FDA Code: HOD / 886.4350) |
• Ophthalmic Forceps (FDA Code: HNR / 886.4350) |
• Ophthalmology, Surgical Instrument Trays |
• Orthopedic Implant, K Nail Measuring Gauge |
• Partial Ossicular Replacement Prosthesis (FDA Code: ETB / 874.3450) A partial ossicular replacement prosthesis is a device intended to be implanted for the functional reconstruction of segments of the ossicular chain and facilitates the conduction of sound wave from the tympanic membrane to the inner ear. The device is made of materials such as stainless steel, tantalum, polytetrafluoroethylene, polyethylene, polytetrafluoroethylene with carbon fibers composite, absorbable gelatin material, porous polyethylene, or from a combination of these materials. |
• Punctum Plug (FDA Code: LZU) |
• Punctum Plugs (Punctal Plugs) |
• Pupil Expander |
• Schirmer Strips (FDA Code: KYD / 886.1800) A Schirmer strip is a device made of filter paper or similar material intended to be inserted under a patient's lower eyelid to stimulate and evaluate formation of tears. |
• Silicone Punctum Plugs |
• smaller punctum plugs |
• Surgical Instrument Tray (FDA Code: FSM / 878.4800) |
• Synthetic Dissolvable Plugs |
• Titanium Ophthalmic Forceps |
• Total Ossicular Replacement Prosthesis (FDA Code: ETA / 874.3495) A total ossicular replacement prosthesis is a device intended to be implanted for the total functional reconstruction of the ossicular chain and facilitates the conduction of sound waves from the tympanic membrance to the inner ear. The device is made of materials such as polytetrafluoroethylene, polytetrafluoroethylene with vitreous carbon fibers composite, porous polyethylene, or from a combination of these materials. |
• Tympanostomy Tube (FDA Code: ETD / 874.3880) A tympanostomy tube is a device that is intended to be implanted for ventilation or drainage of the middle ear. The device is inserted through the tympanic membrane to permit a free exchange of air between the outer ear and middle ear. A type of tympanostomy tube known as the malleous clip tube attaches to the malleous to provide middle ear ventilation. The device is made of materials such as polytetrafluoroethylene, polyethylene, silicon elastomer, or porous polyethylene. |
• Wilder Lacrimal Dilators |