Consulting Wallah › Device Explorer › Endoscopy & surgical instruments › Lumbar interspinous decompression instrument set,
Device Explorer · FDA GUDID · GMDN 47127

Lumbar interspinous decompression instrument set, reusable

A collection of surgical instruments and devices intended to be used for the implantation of an interspinous process decompression (IPD) implant that is inserted between two adjacent lumbar spinous processes during a minimally-invasive procedure to decompress

US‑registered devices577in commercial distribution
Companies10labelers on GUDID
Single‑use6%of device records
Sterile0%labelled sterile
Prescription95%Rx‑only share
ShareLinkedIn

Share of device records

Vb Spine Llc13924%
Xtant Medical Holdings, Inc.13123%
Retropsoas Technologies, Llc10418%
Zavation Llc7914%
Stryker Corporation6511%
Nuvasive, Inc.265%
Companion Spine France183%
Medtronic Sofamor Danek, Inc.81%

Top labelers

CompanyDevicesShare
Vb Spine Llc13924%
Xtant Medical Holdings, Inc.13123%
Retropsoas Technologies, Llc10418%
Zavation Llc7914%
Stryker Corporation6511%
Nuvasive, Inc.265%
Companion Spine France183%
Medtronic Sofamor Danek, Inc.81%
Osseus Fusion Systems, Llc41%
Omnia Medical, Llc31%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

LITe DecompressionARIALITe DECOMPRESSIONCompanion Spine DIAM™ InstrumentationAffixILIFQuadratoOmnia Medical Disc Prep InstrumentsZavationEARP COUNTER RACKEARP, IMPLANT LID 22X50EARP, IMPLANT CADDY 22X50EARP, IMPLANT LID 18X45EARP, IMPLANT LID 18X50EARP INSTRUMENT #2 LIDEARP TRIAL 22x50x14 12°

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

FDA product codes

CodeNameDevices
LXHOrthopedic manual surgical instrument121
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT111
LXHOrthopedic Manual Surgical Instrument89
MNIOrthosis, Spinal Pedicle Fixation66
MNHOrthosis, Spondylolisthesis Spinal Fixation66
KWPAppliance, Fixation, Spinal Interlaminal63

GMDN & GCC registration

  • GMDN code 47127 · non‑implantable
  • Single‑use 6% · sterile 0% · Rx‑only 95% · 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) · 194Outer Diameter (Millimeter) · 100Length (Centimeter) · 48Angle (degree) · 9Width (Millimeter) · 5Height (Millimeter) · 3

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

How many lumbar interspinous decompression instrument set, reusable products are registered in the US?

577 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Lumbar interspinous decompression instrument set, reusable", from 10 companies. The largest labeler is Vb Spine Llc with 24% of records.

Which FDA product codes apply?

LXH (Orthopedic manual surgical instrument), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), LXH (Orthopedic Manual Surgical Instrument), MNI (Orthosis, Spinal Pedicle Fixation)

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?

Add lumbar interspinous decompression instrument set, reusable to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.

Request quotes for Lumbar interspinous decompression instrument set, reusable

Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.

Buying lumbar interspinous decompression instrument set, for a hospital group?Free executive assessment: we benchmark your prices and tender structure against the Network.
Book the free assessment

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.

Get quotes →