Consulting Wallah › Device Explorer › Other devices › Surgical saw blade, reciprocating, reprocessed
Device Explorer · FDA GUDID · GMDN 63598

Surgical saw blade, reciprocating, reprocessed

A flat surgical cutting instrument with a serrated edge, 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 the sternum (not a dedicated sternum saw blade).

US‑registered devices1,773in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Provision1,51786%
Medline Industries, Inc.25114%
Suretek Medical30%
Bioseal20%

Top labelers

CompanyDevicesShare
Provision1,51786%
Medline Industries, Inc.25114%
Suretek Medical30%
Bioseal20%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

StrykerZimmerConMedDe SoutterConMed/LinvatecBrasselerDePuy MitekMicroAireBrasseler USABiometArthrexSynthesConmed/LinvatecWright Medical Technology; Inc.Depuy MitekKomet

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, Surgical1,482
GFABLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL233
GESBlade, Scalpel42
GFFBUR, SURGICAL, GENERAL & PLASTIC SURGERY7
KDGCHISEL (OSTEOTOME)4
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE3

GMDN & GCC registration

  • GMDN code 63598 · 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

No structured size data on the register.

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

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

1,773 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical saw blade, reciprocating, reprocessed", from 4 companies. The largest labeler is Provision with 86% of records.

Which FDA product codes apply?

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

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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