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Device Explorer · FDA GUDID · GMDN 12236

Surgical instrument interim-placement holder, single-use

A device intended to be used in the operating room (OR) by staff to safely hold a hand-held, manual, surgical instrument(s) [e.g., needle, scalpel, scissors, robotic system instrument hand-held remote controller] when not in use during surgery, to avoid damage

US‑registered devices335in commercial distribution
Companies26labelers on GUDID
Single‑use96%of device records
Sterile20%labelled sterile
Prescription74%Rx‑only share
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Share of device records

Novo Surgical, Inc.19458%
Deroyal Industries, Inc.4012%
Xodus Medical, Inc.257%
Bioseal134%
Apollo Medical Products Corp.124%
Medline Industries, Inc.93%
Implantwise Llc72%
Amsino International, Inc.51%

Top labelers

CompanyDevicesShare
Novo Surgical, Inc.19458%
Deroyal Industries, Inc.4012%
Xodus Medical, Inc.257%
Bioseal134%
Apollo Medical Products Corp.124%
Medline Industries, Inc.93%
Implantwise Llc72%
Amsino International, Inc.51%
Aspen Surgical Products, Inc.41%
Medical Action Industries Inc.31%
Itl Asia Pacific Sdn. Bhd.31%
Jb Medical Development, Llc21%

Company = labeler of record on GUDID. 26 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Aspen® Transfer SystemHypoFoamrack-n-stackDriverClip NBMDriverClip SDriverClip UniversalSmartSDGripWelmed, Inc.Novo Surgical Inc.Novo Surgical IncBard-ParkerBard-Parker®Scalpel HolderLiV™ InstrumentsHNM MedicalManus Medical, LLC"NS80715CARD Single Use Magnetic Transfer Zone w

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

FDA product codes

CodeNameDevices
MDMInstrument, Manual, Surgical, General Use196
FSMTRAY, SURGICAL, INSTRUMENT63
KDCINSTRUMENT, SURGICAL, DISPOSABLE22
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE17
KDDKit, surgical instrument, disposable9
GEACannula, Surgical, General & Plastic Surgery8

GMDN & GCC registration

  • GMDN code 12236 · non‑implantable
  • Single‑use 96% · sterile 20% · Rx‑only 74% · 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

Width (Centimeter) · 9Length (Centimeter) · 1

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

How many surgical instrument interim-placement holder, single-use products are registered in the US?

335 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical instrument interim-placement holder, single-use", from 26 companies. The largest labeler is Novo Surgical, Inc. with 58% of records.

Which FDA product codes apply?

MDM (Instrument, Manual, Surgical, General Use), FSM (TRAY, SURGICAL, INSTRUMENT), KDC (INSTRUMENT, SURGICAL, DISPOSABLE), MDM (INSTRUMENT, MANUAL, SURGICAL, GENERAL USE)

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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