Consulting Wallah › Device Explorer › Other devices › Teething device, non-fluid-filled
Device Explorer · FDA GUDID · GMDN 44258

Teething device, non-fluid-filled

A circular or cylindrical device free of fluid and intended to be bitten by a patient (infant or adult) to soothe gums during the teething process. This is a reusable device.

US‑registered devices66in commercial distribution
Companies6labelers on GUDID
Single‑use5%of device records
Sterile0%labelled sterile
Prescription3%Rx‑only share
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Share of device records

Dr. Brown'S Company2741%
Casco Bay Molding Ltd.2335%
Sassy Baby, Inc.1015%
Fourstar Group Inc.35%
Quest Usa Corp.23%
Topco Associates, Llc12%

Top labelers

CompanyDevicesShare
Dr. Brown'S Company2741%
Casco Bay Molding Ltd.2335%
Sassy Baby, Inc.1015%
Fourstar Group Inc.35%
Quest Usa Corp.23%
Topco Associates, Llc12%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Tentacle TeetherOpulent GlobalChewy TubesNUMIDr. Brown'sB.PUREb.pureB. PURESassytippy toes by TopCare

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

FDA product codes

CodeNameDevices
MEFRing, Teething, Non-Fluid Filled99
EFWToothbrush, Manual1

GMDN & GCC registration

  • GMDN code 44258 · non‑implantable
  • Single‑use 5% · sterile 0% · Rx‑only 3% · OTC 5%
  • 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 teething device, non-fluid-filled products are registered in the US?

66 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Teething device, non-fluid-filled", from 6 companies. The largest labeler is Dr. Brown'S Company with 41% of records.

Which FDA product codes apply?

MEF (Ring, Teething, Non-Fluid Filled), EFW (Toothbrush, 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.

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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