Consulting Wallah › Device Explorer › Other devices › Periocular/lacrimal retractor, hand-held, reusable
Device Explorer · FDA GUDID · GMDN 35314

Periocular/lacrimal retractor, hand-held, reusable

A hand-held, non-self-retaining, ophthalmic surgical instrument intended to be used to separate periocular tissues and/or draw aside the margins of a periocular surgical wound during an ophthalmic intervention (e.g., eyelid retraction, lacrimal sac access). Th

US‑registered devices364in commercial distribution
Companies28labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription49%Rx‑only share
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Share of device records

Princeton Medical Group, Inc.11331%
Integra Lifesciences Production Corporation339%
Katena Products, Inc.329%
Aurora Surgical, Llc257%
Hayden Medical, Inc.175%
Krishna Imports Inc175%
Med Saver, Inc.175%
Kls-Martin L.P.134%

Top labelers

CompanyDevicesShare
Princeton Medical Group, Inc.11331%
Integra Lifesciences Production Corporation339%
Katena Products, Inc.329%
Aurora Surgical, Llc257%
Hayden Medical, Inc.175%
Krishna Imports Inc175%
Med Saver, Inc.175%
Kls-Martin L.P.134%
Sontec Instruments, Inc.134%
Geuder Aktiengesellschaft113%
Avalign Technologies, Inc.113%
Steris Corporation103%

Company = labeler of record on GUDID. 28 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Haag Streit John WeissHermann Medizintechnik GmbHN.A.n.a.AESCULAPMORIARETRACTORSPECULUMFELDSTEIN BLEPHAROSTAT RECTANGLESCHACHAR BLEPHAROSTAT LARGESCHACHAR BLEPHAROSTAT SMALLJAEGER STAINLESS STEEL LID PLATESCHEPENS ORBITAL RETRACTORDESMARRES LID RETRACTOR SIZE 3DESMARRES LID RETRACTOR SIZE 2DESMARRES LID RETRACTOR SIZE 1

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

FDA product codes

CodeNameDevices
HNIRetractor, ophthalmic163
GADRetractor111
HNIRetractor, Ophthalmic58
EIGRETRACTOR, ALL TYPES9
HODClamp, eyelid, ophthalmic6
HNCSpecula, ophthalmic6

GMDN & GCC registration

  • GMDN code 35314 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 49% · 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 (Millimeter) · 9Length (Inch) · 9Width (Millimeter) · 8Length (Centimeter) · 4

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

No closely related category with 50+ devices.

How many periocular/lacrimal retractor, hand-held, reusable products are registered in the US?

364 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Periocular/lacrimal retractor, hand-held, reusable", from 28 companies. The largest labeler is Princeton Medical Group, Inc. with 31% of records.

Which FDA product codes apply?

HNI (Retractor, ophthalmic), GAD (Retractor), HNI (Retractor, Ophthalmic), EIG (RETRACTOR, ALL TYPES)

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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