Consulting Wallah › Device Explorer › Other devices › Manual goniometer
Device Explorer · FDA GUDID · GMDN 33651

Manual goniometer

A non-powered, manually-operated measuring device, graduated in degrees (e.g., from 0 to 360 degrees), designed to be used in a clinical setting to measure the range of motion of the limb of a patient by measuring the angle of movement achieved at the joint. I

US‑registered devices67in commercial distribution
Companies28labelers on GUDID
Single‑use3%of device records
Sterile0%labelled sterile
Prescription51%Rx‑only share
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Share of device records

Smith & Nephew, Inc.1015%
Gsource Llc710%
Alimed, Inc.57%
Howmedica Osteonics Corp.46%
Teleflex Incorporated46%
Gf Health Products, Inc.46%
Tornier, Inc.34%
American Diagnostic Corp34%

Top labelers

CompanyDevicesShare
Smith & Nephew, Inc.1015%
Gsource Llc710%
Alimed, Inc.57%
Howmedica Osteonics Corp.46%
Teleflex Incorporated46%
Gf Health Products, Inc.46%
Tornier, Inc.34%
American Diagnostic Corp34%
Novo Surgical, Inc.23%
Avalign Technologies, Inc.23%
Ambler Surgical Corp.23%
Medline Industries, Inc.23%

Company = labeler of record on GUDID. 28 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

INSTRUMENTAESCULAPHumelock Reversed ShoulderTC-100N/ANADONJOYGONIOMETERLafayette Extendable GoniometerAscendNovo Surgical Inc.gSourceMarina MedicalInnomed, Inc.PERFORMANCE HEALTHGONIOMETER PLASTIC CS/10

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

FDA product codes

CodeNameDevices
KQWGoniometer, nonpowered21
KQWGoniometer, Nonpowered17
HRSPLATE, FIXATION, BONE7
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT4
KQWGONIOMETER, NONPOWERED4
HWTTEMPLATE4

GMDN & GCC registration

  • GMDN code 33651 · non‑implantable
  • Single‑use 3% · sterile 0% · Rx‑only 51% · OTC 13%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Centimeter) · 4Lumen/Inner Diameter (Inch) · 3Length (Inch) · 3

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

How many manual goniometer products are registered in the US?

67 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Manual goniometer", from 28 companies. The largest labeler is Smith & Nephew, Inc. with 15% of records.

Which FDA product codes apply?

KQW (Goniometer, nonpowered), KQW (Goniometer, Nonpowered), HRS (PLATE, FIXATION, BONE), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT)

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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