Consulting Wallah › Device Explorer › Other devices › Bone tap, reprocessed
Device Explorer · FDA GUDID · GMDN 61802

Bone tap, reprocessed

A sterile, metal, surgical instrument designed for cutting internal threads into bone so that the threads facilitate the insertion of bone screws. It is made of high-grade stainless steel and has a helical thread intersected with longitudinal cutting grooves f

US‑registered devices54in commercial distribution
Companies3labelers on GUDID
Single‑use11%of device records
Sterile0%labelled sterile
Prescription93%Rx‑only share
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Share of device records

Altus Spine, Llc5296%
Nvision Biomedical Technologies, Inc.12%
Cpm Medical Consultants, Llc12%

Top labelers

CompanyDevicesShare
Altus Spine, Llc5296%
Nvision Biomedical Technologies, Inc.12%
Cpm Medical Consultants, Llc12%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Brickyard Stand-Alone ALIFIndy StandaloneSochiIndyValencia Pedicle Screw SystemAltus Spine Pedicle Screw SystemBoundaryFuse ULTRA Foot plating System

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
GFGBIT, SURGICAL42
KWQAppliance, fixation, spinal intervertebral body27
NKBThoracolumbosacral pedicle screw system24
MAXIntervertebral Fusion Device With Bone Graft, Lumbar12
OVDIntervertebral Fusion Device With Integrated Fixation, Lumba12
HWJAwl10

GMDN & GCC registration

  • GMDN code 61802 · non‑implantable
  • Single‑use 11% · sterile 0% · Rx‑only 93% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 25Outer Diameter (Millimeter) · 24Length (Centimeter) · 3

Use these as the dimensions to specify in a tender line.

How many bone tap, reprocessed products are registered in the US?

54 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone tap, reprocessed", from 3 companies. The largest labeler is Altus Spine, Llc with 96% of records.

Which FDA product codes apply?

GFG (BIT, SURGICAL), KWQ (Appliance, fixation, spinal intervertebral body), NKB (Thoracolumbosacral pedicle screw system), MAX (Intervertebral Fusion Device With Bone Graft, Lumbar)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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