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Device Explorer · FDA GUDID · GMDN 61804

Surgical saw blade, oscillating, reprocessed

A flat surgical cutting instrument, usually made of high-grade stainless steel, with a serrated edge and designed for attachment to a dedicated powered saw used for cutting bone/tissue during orthopaedic or oral surgery; it is not dedicated to cutting through

US‑registered devices279in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Medline Industries, Inc.27097%
Suretek Medical93%

Top labelers

CompanyDevicesShare
Medline Industries, Inc.27097%
Suretek Medical93%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Reprocessed Oscillating Sagittal Saw Blade, ThinReprocessed Small Bone Osc Sagittal Blade, 25 x Reprocessed Small Bone Osc Sagittal Blade, 25 x Reprocessed Medium Narrow Aggressive Blade, 18 xReprocessed Small Bone Osc Sagittal Saw Blade, 1Reprocessed Oscillating Sagittal Saw Blade, 25 xReprocessed Precision Falcon Oscillating BladeReprocessed Oscillating Saw Blade, 19.5 x 90 x 0Reprocessed Stryker Long Narrow Blade, 25 x 5.5mMEDLINEMedlineMEDLINE RENEWAL

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

FDA product codes

CodeNameDevices
GFABLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL629
GFFBUR, SURGICAL, GENERAL & PLASTIC SURGERY24
GFABlade, Saw, General & Plastic Surgery, Surgical9

GMDN & GCC registration

  • GMDN code 61804 · non‑implantable
  • Single‑use 100% · 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

Depth (Millimeter) · 14Width (Millimeter) · 14

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

How many surgical saw blade, oscillating, reprocessed products are registered in the US?

279 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical saw blade, oscillating, reprocessed", from 2 companies. The largest labeler is Medline Industries, Inc. with 97% of records.

Which FDA product codes apply?

GFA (BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL), GFF (BUR, SURGICAL, GENERAL & PLASTIC SURGERY), GFA (Blade, Saw, General & Plastic Surgery, Surgical)

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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