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Device Explorer · FDA GUDID · GMDN 46827

Laryngoscope blade, reusable

The segment of a laryngoscope (i.e., rigid intubation type) intended to be inserted into the oral cavity to manipulate the tongue, preventing it from obstructing the oropharynx and enabling a clear view of the trachea for the insertion of an endotracheal (ET)

US‑registered devices879in commercial distribution
Companies21labelers on GUDID
Single‑use7%of device records
Sterile6%labelled sterile
Prescription48%Rx‑only share
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Share of device records

Sunmed, Llc15718%
Teleflex Incorporated13615%
Maco International9711%
Sklar Corporation9210%
Bound Tree Medical, Llc728%
Flexicare Medical Limited698%
Carnegie Surgical Llc536%
Proact Medical Limited435%

Top labelers

CompanyDevicesShare
Sunmed, Llc15718%
Teleflex Incorporated13615%
Maco International9711%
Sklar Corporation9210%
Bound Tree Medical, Llc728%
Flexicare Medical Limited698%
Carnegie Surgical Llc536%
Proact Medical Limited435%
Jedmed Instrument Company405%
American Medicals314%
Surgical Design, Inc.283%
Heine Optotechnik Gmbh & Co. Kg202%

Company = labeler of record on GUDID. 21 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

IntegraBladeReusable Conventional Blade Mac 1Reusable Conventional Blade Mac 2Reusable Conventional Blade Mac 3Reusable Conventional Blade Mac 4Reusable Conventional Blade Miller Oxy 00Reusable Conventional Blade Miller Oxy 0Reusable Conventional Blade Miller 00Reusable Conventional Blade Miller 0Reusable Conventional Blade Miller 1Reusable Conventional Blade Miller 2Reusable Conventional Blade Miller 3Reusable Conventional Blade Miller 4Reusable Conventional Blade American Mac 1Reusable Conventional Blade American Mac 2Reusable Conventional Blade American Mac 3

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

FDA product codes

CodeNameDevices
CCWLARYNGOSCOPE, RIGID494
CCWLaryngoscope, Rigid429
CCXSUPPORT, PATIENT POSITION2
LRCINSTRUMENT, ENT MANUAL SURGICAL1

GMDN & GCC registration

  • GMDN code 46827 · non‑implantable
  • Single‑use 7% · sterile 6% · Rx‑only 48% · OTC 4%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 179Length (Inch) · 4Depth (Inch) · 2Width (Inch) · 2

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

How many laryngoscope blade, reusable products are registered in the US?

879 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laryngoscope blade, reusable", from 21 companies. The largest labeler is Sunmed, Llc with 18% of records.

Which FDA product codes apply?

CCW (LARYNGOSCOPE, RIGID), CCW (Laryngoscope, Rigid), CCX (SUPPORT, PATIENT POSITION), LRC (INSTRUMENT, ENT MANUAL 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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