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Device Explorer · FDA GUDID · GMDN 33452

Tonsil dissector, reusable

A hand-held surgical instrument, usually spoon-shaped or rounded at the working end, used during the dissection of the tonsils during ear/nose/throat (ENT) surgery. It can be designed in several configurations, e.g., with a shaft that terminates at the distal

US‑registered devices51in commercial distribution
Companies16labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription76%Rx‑only share
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Share of device records

Aesculap, Inc.918%
Sklar Corporation918%
Avalign Technologies, Inc.816%
Fentex Medical Gmbh36%
Rz-Medizintechnik Gmbh36%
Kls-Martin L.P.36%
Med Saver, Inc.36%
Biomet Microfixation, Inc24%

Top labelers

CompanyDevicesShare
Aesculap, Inc.918%
Sklar Corporation918%
Avalign Technologies, Inc.816%
Fentex Medical Gmbh36%
Rz-Medizintechnik Gmbh36%
Kls-Martin L.P.36%
Med Saver, Inc.36%
Biomet Microfixation, Inc24%
Br Surgical, Llc24%
Teleflex Incorporated24%
Steris Corporation24%
Spiggle & Theis Medizintechnik Gmbh12%

Company = labeler of record on GUDID. 16 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

FENTEXMcDonald dissectorRZ Medizintechnik GmbHAESCULAPDISSECTORPRINCETONELMEDN/ABR Surgical, LLCMSI Precision Specialty InstrumentsHURD TONSIL DSSECTOR/PILLAR RETRACTORMillenniumAvalignPILLINGV. MuellerJEDMED

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

FDA product codes

CodeNameDevices
KBMDISSECTOR, TONSIL18
KBRNEEDLE, TONSIL SUTURING12
KCBTUBE, TONSIL SUCTION6
LRCINSTRUMENT, ENT MANUAL SURGICAL4
GDLNEEDLE, SUTURING, REUSABLE3
KBMDissector, Tonsil3

GMDN & GCC registration

  • GMDN code 33452 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 76% · 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

Length (Inch) · 1

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

How many tonsil dissector, reusable products are registered in the US?

51 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tonsil dissector, reusable", from 16 companies. The largest labeler is Aesculap, Inc. with 18% of records.

Which FDA product codes apply?

KBM (DISSECTOR, TONSIL), KBR (NEEDLE, TONSIL SUTURING), KCB (TUBE, TONSIL SUCTION), 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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