Consulting Wallah › Device Explorer › Other devices › Bone-resection orthopaedic reamer, reprocessed
Device Explorer · FDA GUDID · GMDN 61806

Bone-resection orthopaedic reamer, reprocessed

An orthopaedic surgical instrument designed to resect bone (cut out part of the bone) and precisely shape a specific area of bone as it is advanced for the acceptance of a prosthetic implant, typically at or within a joint (e.g., condyle of knee, neck of humer

US‑registered devices86in commercial distribution
Companies3labelers on GUDID
Single‑use98%of device records
Sterile98%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Medline Industries, Inc.7992%
Crossroads Extremity Systems56%
Stryker Gmbh22%

Top labelers

CompanyDevicesShare
Medline Industries, Inc.7992%
Crossroads Extremity Systems56%
Stryker Gmbh22%

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

Brand names on the register (sample)

REUNIONMotoBAND™ CP DynaForce®MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer MotoBAND™ CP DynaForce® MPJ Cup and Cone Reamer MedlineMEDLINE RENEWALMEDLINE

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

FDA product codes

CodeNameDevices
HTOREAMER53
HTSKNIFE, ORTHOPEDIC22
HTOReamer5
HRSPlate, Fixation, Bone3
HWCScrew, Fixation, Bone3
GFFBUR, SURGICAL, GENERAL & PLASTIC SURGERY3

GMDN & GCC registration

  • GMDN code 61806 · non‑implantable
  • Single‑use 98% · sterile 98% · Rx‑only 100% · 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

Outer Diameter (Millimeter) · 1

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

How many bone-resection orthopaedic reamer, reprocessed products are registered in the US?

86 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Bone-resection orthopaedic reamer, reprocessed", from 3 companies. The largest labeler is Medline Industries, Inc. with 92% of records.

Which FDA product codes apply?

HTO (REAMER), HTS (KNIFE, ORTHOPEDIC), HTO (Reamer), HRS (Plate, Fixation, Bone)

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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