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Device Explorer · FDA GUDID · GMDN 15774

Cast cutter blade

A surgical cutting device intended to be used with a cast removal tool (cast cutter) to provide the cutting edge for cutting through cast material so that this can be removed from the patient. It is formed as a thin, rounded, half moon-like, or circular blade

US‑registered devices50in commercial distribution
Companies4labelers on GUDID
Single‑use88%of device records
Sterile0%labelled sterile
Prescription100%Rx‑only share
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Share of device records

De Soutter Medical Limited3468%
Omega Surgical Instruments Inc1020%
Integra Lifesciences Production Corporation48%
Boss Instruments, Ltd., Inc.24%

Top labelers

CompanyDevicesShare
De Soutter Medical Limited3468%
Omega Surgical Instruments Inc1020%
Integra Lifesciences Production Corporation48%
Boss Instruments, Ltd., Inc.24%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

De Soutter MedicalBOSS InstrumentsN/AIntegra® Jarit®Integra® Miltex®

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

FDA product codes

CodeNameDevices
LGHInstrument, Cast Removal, Ac-Powered35
GFABlade, Saw, General & Plastic Surgery, Surgical10
LGHINSTRUMENT, CAST REMOVAL, AC-POWERED6
LGGINSTRUMENT, CAST APPLICATION/REMOVAL, MANUAL6
GESBlade, Scalpel1

GMDN & GCC registration

  • GMDN code 15774 · non‑implantable
  • Single‑use 88% · sterile 0% · 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

Width (Millimeter) · 4Length (Millimeter) · 1

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

How many cast cutter blade products are registered in the US?

50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cast cutter blade", from 4 companies. The largest labeler is De Soutter Medical Limited with 68% of records.

Which FDA product codes apply?

LGH (Instrument, Cast Removal, Ac-Powered), GFA (Blade, Saw, General & Plastic Surgery, Surgical), LGH (INSTRUMENT, CAST REMOVAL, AC-POWERED), LGG (INSTRUMENT, CAST APPLICATION/REMOVAL, MANUAL)

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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