FEMORAL HEAD REMOVER MANUFACTURED BY BIOMET, INC.

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Request for Information Form	Contact Information
Company Name	BIOMET, INC.
Address	56 EAST BELL DR. P.O. BOX 587
City, State, Zip	WARSAW, IN 46581
Country	US
FDA Owner/Operator Phone	574-267-6639
FDA Medical Specialty Code	OR - Orthopedic
FDA Product Code	HWI
FDA Classification Name	CORKSCREW
FDA Device Classification Code	General Controls
FDA Regulation Number	888.4540
FDA Common Generic Name	FEMORAL HEAD REMOVER
FDA Proprietary Device Name	FEMORAL HEAD REMOVER
FDA Owner / Operator Number	1825034
FDA Owner / Operator Name	BIOMET, INC.
FDA Establishment Registration Number	1825034
FDA Registered Establishment Name	BIOMET, INC.
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date
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	AESCULAP AG & CO. KG. AM AESCULAP PLATZ TUTTLINGEN, DONAU, D-78532 GM 49-74-6195-1548 / 610-984-9074	CORKSCREW	VARIOUS MODELS
2	B. BRAUN MEDICAL LTD 43 ALLEN ST. SHEFFIELD, SOUTH YORKSHIRE, S3 7AX UK 044-114-2259200 / 011-422-59200	MULTIPLE	VARIOUS
3	DEPUY INTL., LTD. ST. ANTHONY'S RD. LEEDS, LS11 8DT UK 574-267-8143 4906 / 574-371-4906	WROBLEWSKI FEMORAL CEMENT REMOVER	WROBLEWSKI FEMORAL CEMENT REMOVER
4	WALDEMAR LINK GMBH & CO. KG BARKHAUSENWEG 10 HAMBURG, 22339 GM / 40-539-95-0 *240	CORKSCREW	CORKSCREW
5	ZIMMER TRABECULAR METAL TECHNOLOGY 10 POMEROY RD. PARSIPPANY, NJ 07054 US 800-613-6131 / 201-818-1800	ACETABULAR INSERT REMOVER	ACETABULAR INSERT REMOVER
6	ZIMMER, INC. 345 E. MAIN ST. WARSAW, IN 46580 US 800-613-6131 / 574-372-4485	MULTIPLE	CORKSCREWS