Gulden Ophthalmics

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Contact: Richard Wehr - Director of Marketing
Web: http://www.guldenindustries.com
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Address: 225 Cadwalader Avenue, Elkins Park, Pennsylvania 19027, USA
Phone: +1-(215)-884-8105, 800-659-2250 | Fax: +1-(215)-884-0418 | Map/Directions >>

Profile: Gulden Ophthalmic is a manufacturer of ophthalmic instruments and devices. Our product list comprises of cornea eye models, detachment eye models and lighted low vision pens. Our lighted low vision pen assists in writing for a low vision patient. The magnification offered is 2 x. It has an adjustable lens. Our detachemnt eye model is a realistic model of the human eye for patient education. It shows vitreous and retinal detachments & increases patient understanding.

The company was founded in 1938, has revenues of < USD 1 Million and is ISO 9002, CE certified.

FDA Registration Number: 2518410

37 Products/Services (Click for related suppliers)

• AC-Powered Pupillometer (FDA Code: HLG / 886.1700)

A pupillometer is an AC-powered or manual device intended to measure by reflected light the width or diameter of the pupil of the eye.

• Amsler Grid (FDA Code: HOQ / 886.1330)

An Amsler grid is a device that is a series of charts with grids of different sizes that are held at 30 centimeters distance from the patient and intended to rapidly detect central and paracentral irregularities in the visual field.

• Battery-Powered Spectacle Dissociation Test (FDA Code: HLO / 886.1910)

A spectacle dissociation test system is an AC-powered or battery-powered device, such as a Lancaster test system, that consists of a light source and various filters, usually red or green filters, intended to subjectively measure imbalance of ocular muscles.

• Biophotometer/Adaptometer (FDA Code: HJW / 886.1050)

An adaptometer (biophotometer) is an AC-powered device that provides a stimulating light source which has various controlled intensities intended to measure the time required for retinal adaptation (regeneration of the visual purple) and the minimum light threshold.

• Color Vision Tester (FDA Code: HIT / 886.1170)

A color vision tester is a device that consists of various colored materials, such as colored yarns or color vision plates (multicolored plates which patients with color vision deficiency would perceive as being of one color), intended to evaluate color vision.

• 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).

• Eye Gel Mask

• Eye Guards

• Eye Shields

• Eye Sphere Implant (FDA Code: HPZ / 886.3320)

An eye sphere implant is a device intended to be implanted in the eyeball to occupy space following the removal of the contents of the eyeball with the sclera left intact.

• Eye Tonometer

• Fusion and Stereoscopic Target (FDA Code: HLP / 886.1880)

A fusion and stereoscopic target is a device intended for use as a viewing object with a stereoscope (886.1870).

• Gel Eye Shields

• Human Eye Model

• Low Vision devices

• Low-Vision Hand-Held Magnifier (FDA Code: HJF / 886.5540)

A low-vision magnifier is a device that consists of a magnifying lens intended for use by a patient who has impaired vision. The device may be held in the hand or attached to spectacles.

• Maddox Lens (FDA Code: HKR / 886.1400)

A Maddox lens is a device that is a series of red cylinders that change the size, shape, and color of an image. The device is intended to be handheld or placed in a trial frame to evaluate eye muscle dysfunction.

• Nearpoint Ruler (FDA Code: HLE / 886.1790)

A nearpoint ruler is a device calibrated in centimeters intended to measure the nearpoint of convergence (the point to which the visual lines are directed when convergence is at its maximum).

• Non-Custom Artificial Eye (FDA Code: HQH / 886.3200)

An artificial eye is a device resembling the anterior portion of the eye, usually made of glass or plastic, intended to be inserted in a patient's eye socket anterior to an orbital implant, or the eviscerated eyeball, for cosmetic purposes. The device is not intended to be implanted.

• Occluders

• Ophthalmic AC-Powered Fixation Device (FDA Code: HPL / 886.1290)

A fixation device is an AC-powered device intended for use as a fixation target for the patient during ophthalmological examination. The patient directs his or her gaze so that the visual image of the object falls on the fovea centralis (the center of the macular retina of the eye.)

• Ophthalmic Aspiration Cannula (FDA Code: HMX / 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.

• Ophthalmic Cannula (FDA Code: HMX / 886.4350)

• Ophthalmic Conformer (FDA Code: HQN / 886.3130)

An ophthalmic conformer is a device usually made of molded plastic intended to be inserted temporarily between the eyeball and eyelid to maintain space in the orbital cavity and prevent closure or adhesions during the healing process following surgery. ]

• 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 Images Storage Device (FDA Code: NFF / 892.2010)

A medical image storage device is a device that provides electronic storage and retrieval functions for medical images. Examples include devices employing magnetic and optical discs, magnetic tape, and digital memory.

• Ophthalmic Prism Bar (FDA Code: HKW / 886.1650)

An ophthalmic bar prism is a device that is a bar composed of fused prisms of gradually increasing strengths intended to measure latent and manifest strabismus (eye muscle deviation) or the power of fusion of a patient's eyes.

• Ophthalmic Spud (FDA Code: HNA / 886.4350)

• Ophthalmic Trial Lens Clip (FDA Code: HPB / 886.1410)

An ophthalmic trial lens clip is a device intended to hold prisms, spheres, cylinders, or occluders on a trial frame or spectacles for vision testing.

• Ophthalmic Trial Lens Set (FDA Code: HPC / 886.1405)

An ophthalmic trial lens set is a device that is a set of lenses of various dioptric powers intended to be handheld or inserted in a trial frame for vision testing to determine refraction.

• Opthalmic Surgical Instruments

• Opticokinetic Drum (FDA Code: HOW / 886.1200)

An optokinetic drum is a drum-like device covered with alternating white and dark stripes or pictures that can be rotated on its handle. The device is intended to elicit and evaluate nystagmus (involuntary rapid movement of the eyeball) in patients.

• Skiascopic Rack (FDA Code: HMH / 886.1750)

A skiascopic rack is a device that is a rack and a set of attached ophthalmic lenses of various dioptric strengths intended as an aid in refraction.

• Stereopsis Measuring Instrument (FDA Code: HLC / 886.1460)

A stereopsis measuring instrument is a device intended to measure depth perception by illumination of objects placed on different planes.

• Surgical Ophthalmic Cannula (FDA Code: HMX / 886.4350)

• Tonometers

• Visual Acuity Charts (FDA Code: HOX / 886.1150)

A visual acuity chart is a device that is a chart, such as a Snellen chart with block letters or other symbols in graduated sizes, intended to test visual acuity.