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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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Arthrex® - 00888867037991

IBAL UKA,TIB SIZING GD,SZ 1,RM
ARTHREX, INC.
AR-601-TTR1
In Commercial Distribution

  • 00888867037991 ()
AR-601-TTR1

  • Suturing unit, single-use

Arthrex® - 00888867037984

IBAL UKA,TIB SIZING GD,SZ 6,LM
ARTHREX, INC.
AR-601-TTL6
In Commercial Distribution

  • 00888867037984 ()
AR-601-TTL6

  • Suturing unit, single-use

Arthrex® - 00888867037977

IBAL UKA,TIB SIZING GD,SZ 5,LM
ARTHREX, INC.
AR-601-TTL5
In Commercial Distribution

  • 00888867037977 ()
AR-601-TTL5

  • Suturing unit, single-use

Arthrex® - 00888867037960

IBAL UKA,TIB SIZING GD,SZ 4,LM
ARTHREX, INC.
AR-601-TTL4
In Commercial Distribution

  • 00888867037960 ()
AR-601-TTL4

  • Suturing unit, single-use

Arthrex® - 00888867037953

IBAL UKA,TIB SIZING GD,SZ 3,LM
ARTHREX, INC.
AR-601-TTL3
In Commercial Distribution

  • 00888867037953 ()
AR-601-TTL3

  • Suturing unit, single-use

Arthrex® - 00888867037946

IBAL UKA,TIB SIZING GD,SZ 2,LM
ARTHREX, INC.
AR-601-TTL2
In Commercial Distribution

  • 00888867037946 ()
AR-601-TTL2

  • Suturing unit, single-use

Arthrex® - 00888867037939

IBAL UKA,TIB SIZING GD,SZ 1,LM
ARTHREX, INC.
AR-601-TTL1
In Commercial Distribution

  • 00888867037939 ()
AR-601-TTL1

  • Suturing unit, single-use

Arthrex® - 00888867037908

iBALANCE UKA, RESECTION GUIDE, RIGHT
ARTHREX, INC.
AR-601-TRRM
In Commercial Distribution

  • 00888867037908 ()
AR-601-TRRM

  • Device sterilization/disinfection container, reusable

Arthrex® - 00888867037892

iBALANCE UKA, RESECTION GUIDE, LEFT
ARTHREX, INC.
AR-601-TRLM
In Commercial Distribution

  • 00888867037892 ()
AR-601-TRLM

  • Device sterilization/disinfection container, reusable

Arthrex® - 00888867037830

iBALANCE UKA, TIBIAL ALIGNMENT GUIDE
ARTHREX, INC.
AR-601-TG00
In Commercial Distribution

  • 00888867037830 ()
AR-601-TG00

  • Suturing unit, single-use

Arthrex® - 00888867037311

IBAL UKA,POST RESECT GD,10MM
ARTHREX, INC.
AR-601-PB10
In Commercial Distribution

  • 00888867037311 ()
AR-601-PB10

  • Suturing unit, single-use

Arthrex® - 00888867037304

IBAL UKA,POST RESECT GD,9MM
ARTHREX, INC.
AR-601-PB09
In Commercial Distribution

  • 00888867037304 ()
AR-601-PB09

  • Suturing unit, single-use

Arthrex® - 00888867037281

IBAL UKA,POST RESCTION GD,7MM
ARTHREX, INC.
AR-601-PB07
In Commercial Distribution

  • 00888867037281 ()
AR-601-PB07

  • Suturing unit, single-use

Arthrex® - 00888867037274

IBAL UKA,POST RESECT GD,6MM
ARTHREX, INC.
AR-601-PB06
In Commercial Distribution

  • 00888867037274 ()
AR-601-PB06

  • Suturing unit, single-use

Arthrex® - 00888867037267

IBAL UKA,POST RESECT GD,5MM
ARTHREX, INC.
AR-601-PB05
In Commercial Distribution

  • 00888867037267 ()
AR-601-PB05

  • Suturing unit, single-use

Arthrex® - 00888867037250

IBAL UKA,POST RESECT GD,4MM
ARTHREX, INC.
AR-601-PB04
In Commercial Distribution

  • 00888867037250 ()
AR-601-PB04

  • Suturing unit, single-use

Arthrex® - 00888867037243

IBAL UKA,POST RESECT GD,3MM
ARTHREX, INC.
AR-601-PB03
In Commercial Distribution

  • 00888867037243 ()
AR-601-PB03

  • Suturing unit, single-use

Arthrex® - 00888867037298

IBAL UKA,POST RESECT GD,8MM
ARTHREX, INC.
AR-601-PB08
In Commercial Distribution

  • 00888867037298 ()
AR-601-PB08

  • Suturing unit, single-use

Arthrex® - 00888867036994

IBAL UKA,CHAMFER & PEG GD,SZ 6,RM/LL
ARTHREX, INC.
AR-601-CRMF
In Commercial Distribution

  • 00888867036994 ()
AR-601-CRMF

  • Arthroscopic shaver system blade, reusable

Arthrex® - 00888867036987

IBAL UKA,CHAMFER & PEG GD,SZ 5,RM/LL
ARTHREX, INC.
AR-601-CRME
In Commercial Distribution

  • 00888867036987 ()
AR-601-CRME

  • Bone lever/elevator, reusable
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