Consulting Wallah › Device Explorer › Ophthalmic › Soft corrective contact lens, extended-wear
Device Explorer · FDA GUDID · GMDN 47843

Soft corrective contact lens, extended-wear

A soft ophthalmic lens intended to be worn directly against the cornea and adjacent limbal and scleral areas of the eye to correct refractive vision conditions (e.g., myopia, hyperopia, astigmatism, presbyopia); it is designed for continuous overnight wear ran

US‑registered devices60in commercial distribution
Companies1labelers on GUDID
Single‑use0%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Vizionfocus Inc.60100%

Top labelers

CompanyDevicesShare
Vizionfocus Inc.60100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

IDEAL SiHy/1Month/6PK

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

FDA product codes

CodeNameDevices
LPLLenses, Soft Contact, Daily Wear60
MVNLens, Contact, (Disposable)60

GMDN & GCC registration

  • GMDN code 47843 · non‑implantable
  • Single‑use 0% · sterile 100% · 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

No structured size data on the register.

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

How many soft corrective contact lens, extended-wear products are registered in the US?

60 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Soft corrective contact lens, extended-wear", from 1 companies. The largest labeler is Vizionfocus Inc. with 100% of records.

Which FDA product codes apply?

LPL (Lenses, Soft Contact, Daily Wear), MVN (Lens, Contact, (Disposable))

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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