HEMEDEX FIXATION DEVICE MANUFACTURED BY HEMEDEX INCORPORATED

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Request for Information Form	Contact Information
Company Name	HEMEDEX INCORPORATED
Address	222 THIRD ST., SUITE 0123
City, State, Zip	CAMBRIDGE, MA 02142
Country	US
FDA Owner/Operator Phone	617-577-1759
FDA Medical Specialty Code	OR - Orthopedic
FDA Product Code	KYN
FDA Classification Name	PROSTHESIS, WRIST, CONSTRAINED, METAL
FDA Device Classification Code	Premarket Approval
FDA Regulation Number	888.3790
FDA Common Generic Name	CATHETER/PROBE FIXATION DEVICE
FDA Proprietary Device Name	HEMEDEX FIXATION DEVICE
FDA Owner / Operator Number	9048090
FDA Owner / Operator Name	HEMEDEX INCORPORATED
FDA Establishment Registration Number	3003730855
FDA Registered Establishment Name	HEMEDEX INCORPORATED
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	07-03-04
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 companyies may manufacture a similar device.

	Company Name / Address / Phone	Proprietary Device Name	Common Generic Device Name
1	BANYAN HEALTH CARE PRODUCTS, INC. 10058 SPANISH ISLES BLVD. #F-6 BOCA RATON, FL 33498 US 561-852-1400 414 / 561-852-1400 414	PROSTHESIS, WRIST, CONSTRAINED, METAL	WRIST SPLINT