Consulting Wallah › Device Explorer › Other devices › Percussion hammer, manual, reusable
Device Explorer · FDA GUDID · GMDN 11950

Percussion hammer, manual, reusable

A hand-held manual instrument designed to be used by an examining physician to gently tap near a patient's joints to test reflexes (e.g., patellar, ankle reflexes). It consists of a handle and shaft typically made of stainless steel, and has a head that may be

US‑registered devices229in commercial distribution
Companies29labelers on GUDID
Single‑use7%of device records
Sterile1%labelled sterile
Prescription32%Rx‑only share
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Share of device records

Sklar Corporation4520%
Medicon Eg. Chirurgiemechaniker-Genossenschaft209%
American Diagnostic Corp209%
Novo Surgical, Inc.198%
Princeton Medical Group, Inc.167%
Mdf Instruments Medifriend Inc.157%
Rashman Corporation146%
Bv Medical125%

Top labelers

CompanyDevicesShare
Sklar Corporation4520%
Medicon Eg. Chirurgiemechaniker-Genossenschaft209%
American Diagnostic Corp209%
Novo Surgical, Inc.198%
Princeton Medical Group, Inc.167%
Mdf Instruments Medifriend Inc.157%
Rashman Corporation146%
Bv Medical125%
Integra Lifesciences Production Corporation115%
American Medicals83%
Br Surgical, Llc73%
Steris Corporation73%

Company = labeler of record on GUDID. 29 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

PediaPalsEMSRUNTealmedMDF®MaxMoreSpineRZ Medizintechnik GmbHAESCULAPMediconBV MedicalNovo Surgical Inc.gSourceBR Surgical, LLCPRINCETONHammerPrestige Medicalhammer

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

FDA product codes

CodeNameDevices
GWZPercussor71
FZYHAMMER, SURGICAL57
GWZPERCUSSOR41
FZYHammer, Surgical27
HXLMallet14
HNHRing, Ophthalmic (Flieringa)8

GMDN & GCC registration

  • GMDN code 11950 · non‑implantable
  • Single‑use 7% · sterile 1% · Rx‑only 32% · OTC 9%
  • 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) · 4Length (Inch) · 3

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

No closely related category with 50+ devices.

How many percussion hammer, manual, reusable products are registered in the US?

229 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Percussion hammer, manual, reusable", from 29 companies. The largest labeler is Sklar Corporation with 20% of records.

Which FDA product codes apply?

GWZ (Percussor), FZY (HAMMER, SURGICAL), GWZ (PERCUSSOR), FZY (Hammer, Surgical)

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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