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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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LLIF CUP CURETTE, UP, SERRATED
HYHTE HOLDINGS, INC.
GZB13SP03
In Commercial Distribution

  • 00841379187011 ()

  • 3
GZB13SP03

  • Bone curette, reusable
LLIF CUP CURETTE, UP, SERRATED
HYHTE HOLDINGS, INC.
GZB13SP02
In Commercial Distribution

  • 00841379187004 ()

  • 2
GZB13SP02

  • Bone curette, reusable
LLIF CUP CURETTE, UP, SERRATED
HYHTE HOLDINGS, INC.
GZB13SP01
In Commercial Distribution

  • 00841379186991 ()

  • 1
GZB13SP01

  • Bone curette, reusable
LLIF CUP CURETTE, UP
HYHTE HOLDINGS, INC.
GZB13SG06
In Commercial Distribution

  • 00841379186984 ()

  • 6
GZB13SG06

  • Bone curette, reusable
LLIF CUP CURETTE, UP
HYHTE HOLDINGS, INC.
GZB13SG05
In Commercial Distribution

  • 00841379186977 ()

  • 5
GZB13SG05

  • Bone curette, reusable
LLIF CUP CURETTE, UP
HYHTE HOLDINGS, INC.
GZB13SG04
In Commercial Distribution

  • 00841379186960 ()

  • 4
GZB13SG04

  • Bone curette, reusable
LLIF CUP CURETTE, UP
HYHTE HOLDINGS, INC.
GZB13SG03
In Commercial Distribution

  • 00841379186953 ()

  • 3
GZB13SG03

  • Bone curette, reusable
LLIF CUP CURETTE, UP
HYHTE HOLDINGS, INC.
GZB13SG02
In Commercial Distribution

  • 00841379186946 ()

  • 2
GZB13SG02

  • Bone curette, reusable
LLIF CUP CURETTE, UP
HYHTE HOLDINGS, INC.
GZB13SG01
In Commercial Distribution

  • 00841379186939 ()

  • 1
GZB13SG01

  • Bone curette, reusable
LLIF CUP CURETTE, ANGLED, HIGH, CAUDAL, SERRATED
HYHTE HOLDINGS, INC.
GZB13AN06
In Commercial Distribution

  • 00841379186922 ()

  • 6
GZB13AN06

  • Bone curette, reusable
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