SURGICUTT INCISION DEVICE MANUFACTURED BY INTERNATIONAL TECHNIDYNE CORPORATION

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Request for Information Form	Contact Information
Company Name	INTERNATIONAL TECHNIDYNE CORPORATION
Address	20 CORPORATE PLACE SOUTH
City, State, Zip	PISCATAWAY, NJ 08854
Country	US
FDA Owner/Operator Phone	732-548-5700
FDA Medical Specialty Code	HE - Hematology
FDA Product Code	JCA
FDA Classification Name	DEVICE, BLEEDING TIME
FDA Device Classification Code	Standards
FDA Regulation Number	864.6100
FDA Common Generic Name	INCISION DEVICE
FDA Proprietary Device Name	SURGICUTT INCISION DEVICE
FDA Owner / Operator Number	2250033
FDA Owner / Operator Name	INTERNATIONAL TECHNIDYNE CORPORATION
FDA Establishment Registration Number	3005776351
FDA Registered Establishment Name	INTERNATIONAL TECHNIDYNE CORPORATION
FDA Operation Code(s)	MS - Specification Developer
FDA Listing Date	05-24-06
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	HELENA LABORATORIES 1530 LINDBERGH DR. BEAUMONT, TX 77704 US 409-842-3714 / 409-842-3714 271	TRIPLETT BLEEDING TIME TEST DEVICE	BLEEDING TIME TEST DEVICE
2	INTERNATIONAL TECHNIDYNE CORP. 23 NEVSKY ST. EDISON, NJ 08820 US 732-548-5700 / 732-548-5700 265	SURGICUTT, -2, -JR, -NEWBORN	INCISION DEVICES, VARIOUS
3	INTERNATIONAL TECHNIDYNE CORPORATION 330 TALMADGE RD. EDISON, NJ 08820 US 732-548-5700 / 732-548-5700 265	SURGICUTT INCISION DEVICE	INCISION DEVICE