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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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Pisces-SA - B0621750M170

26x35x17, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M170
In Commercial Distribution

  • B0621750M170 ()
1750-M170

  • Surgical instrument/implant depth limiter, reusable

Pisces-SA - B0621750M150

26x35x15, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M150
In Commercial Distribution

  • B0621750M150 ()
1750-M150

  • Abdominal/ENT/orthopaedic surgical probe, reusable

Pisces-SA - B0621750M130

26x35x13, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M130
In Commercial Distribution

  • B0621750M130 ()
1750-M130

  • Surgical instrument/implant depth limiter, reusable

Pisces-SA - B0621750M110

26x35x11, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-M110
In Commercial Distribution

  • B0621750M110 ()
1750-M110

  • Surgical instrument/implant depth limiter, reusable

Pisces-SA - B0621750L190

29x39x19, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L190
In Commercial Distribution

  • B0621750L190 ()
1750-L190

  • Surgical instrument/implant depth limiter, reusable

Pisces-SA - B0621750L150

29x39x15, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L150
In Commercial Distribution

  • B0621750L150 ()
1750-L150

  • Surgical instrument/implant depth limiter, reusable

Pisces-SA - B0621750L130

29x39x13, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L130
In Commercial Distribution

  • B0621750L130 ()
1750-L130

  • Surgical instrument/implant depth limiter, reusable

Pisces-SA - B0621750L110

29x39x11, 20°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L110
In Commercial Distribution

  • B0621750L110 ()
1750-L110

  • Surgical instrument/implant depth limiter, reusable

Hedstrom-Files - E2250730280201

HEDSTROM FILES 28MM 20
TULSA DENTAL PRODUCTS LLC
07328020R
In Commercial Distribution

  • E2250730280200 ()
  • E2250730280201 ()
07328020R

  • Manual endodontic file/rasp, single-use

NITI K-FILES - E2250620250201

NI-TI K-FILES 25MM 20
TULSA DENTAL PRODUCTS LLC
2632520
In Commercial Distribution

  • E2250620250200 ()
  • E2250620250201 ()
2632520

  • Rotary/reciprocating endodontic file/rasp, single-use
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