Consulting Wallah › Device Explorer › Other devices › Podiatric bur, single-use
Device Explorer · FDA GUDID · GMDN 64025

Podiatric bur, single-use

A rotary abrasive device typically used by a podiatrist intended to debride excrescences and treat conditions such as heavy toenails and/or plantar calluses. It consists of a well-differentiated head of various shapes (e.g., cone, cylinder, inverted cone, pear

US‑registered devices73in commercial distribution
Companies5labelers on GUDID
Single‑use89%of device records
Sterile62%labelled sterile
Prescription30%Rx‑only share
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Share of device records

Lukas-Erzett Gmbh & Co. Kg2636%
American Medicals2534%
Omega Surgical Instruments Inc811%
Bailey Instruments Ltd710%
Robinson Healthcare Limited710%

Top labelers

CompanyDevicesShare
Lukas-Erzett Gmbh & Co. Kg2636%
American Medicals2534%
Omega Surgical Instruments Inc811%
Bailey Instruments Ltd710%
Robinson Healthcare Limited710%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Susol® Diamond Bur 1HP EnucleatorSusol® Diamond Bur 15CSusol® Diamond Bur Pear 1Susol® Diamond Bur Bud 2Susol® Diamond Bur Bud 1Susol® Diamond Bur Pear 2Susol® Diamond Bur Bud 3Instrapac"GT PODO 0.512 in (13 mm) round Shank 3/32""""GT PODO 0.394 in (10 mm) pointed Shank 3/32""""GT PODO 0.276 in (7 mm) pointed Shank 3/32""""GT PODO 0.276 in (7 mm) round Shank 3/32""""GT PODO 0.197 in (5 mm) round Shank 3/32""""GT PODO 0.394 in (10 mm) round Shank 3/32"""N/AAmerican Medicals

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

FDA product codes

CodeNameDevices
GFFBur, Surgical, General & Plastic Surgery73

GMDN & GCC registration

  • GMDN code 64025 · non‑implantable
  • Single‑use 89% · sterile 62% · Rx‑only 30% · OTC 36%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

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

How many podiatric bur, single-use products are registered in the US?

73 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Podiatric bur, single-use", from 5 companies. The largest labeler is Lukas-Erzett Gmbh & Co. Kg with 36% of records.

Which FDA product codes apply?

GFF (Bur, Surgical, General & Plastic Surgery)

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.

How do I get quotes?

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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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