RENAISSANCE AUTO KERATOMETER MANUFACTURED BY ALCON MANUFACTURING, LTD.

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Request for Information Form	Contact Information
Company Name	ALCON MANUFACTURING, LTD.
Address	15800 ALTON PKWY.
City, State, Zip	IRVINE, CA 92618
Country	US
FDA Owner/Operator Phone	817-551-6813
FDA Medical Specialty Code	OP - Opthalmic
FDA Product Code	HLR
FDA Classification Name	KERATOSCOPE, BATTERY-POWERED
FDA Device Classification Code	General Controls
FDA Regulation Number	886.1350
FDA Common Generic Name	KERATOMETER
FDA Proprietary Device Name	RENAISSANCE AUTO KERATOMETER
FDA Owner / Operator Number	1610287
FDA Owner / Operator Name	ALCON MANUFACTURING, LTD.
FDA Establishment Registration Number	2028159
FDA Registered Establishment Name	ALCON MANUFACTURING, LTD.
FDA Operation Code(s)	MM - Manufacturer MS - Specification Developer
FDA Listing Date	01-14-94
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

Our records indicate that the following medical device companies may manufacture a similar device.

	Company Name / Address / Phone	Proprietary Device Name	Common Generic Device Name
1	CARTON OPTICAL INDUSTRIES, LTD. 27-11, HIGASHI UENO 1-CHOME, TAITO-KU TOKYO, 110-0015 JA 03-38-32-1320 / 410-793-0484	MULTIPLE	KERATOSCOPE BATTERY POWERED
2	JEDMED INSTRUMENT CO. 5416 JEDMED CT. ST. LOUIS, MO 63129 US 314-845-3770 / 314-845-3770 220	KERATOSCOPE	KERATOSCOPE
3	KEELER INSTRUMENTS, INC. 456 PKWY. BROOMALL, PA 19008 US 610-353-4350 / 610-353-4350
4	NIKON INC. 1300 WALT WHITMAN RD. MELVILLE, NY 11747 US 631-547-4200 / 631-547-4200 4251	RETINOMAX K-PLUS AUTO REFACT/KERATOMETER	RETINOMAX K-PLUS AUTO REFACT/KERATOMETER