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S.B.M

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S.B.M is a medical device manufacturer, with 447 devices listed in FDA GUDID and EUDAMED (FDA Class II and I) as of 12 Nov 2026.

Devices
447

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 447
  • EUDAMED 225

A device listed in two registries counts in both.

Device classes
  • FDA Class II 299
  • FDA Class I 148
Identifiers
  • DUNS 772462123

What S.B.M makes

The company manufactures bioabsorbable and non-bioabsorbable orthopaedic bone screws and tendon/ligament anchors, reusable arthroscopic surgical tools including drill bits, guidewires, and depth gauges, as well as synthetic bone graft materials and reusable arthroscopic procedure kits. Their portfolio also includes knotless tendon/ligament fixation systems and specialized implants designed for orthopaedic and sports medicine applications.

The devices fall under FDA Class I and Class II classifications and are listed in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States, adhering to applicable regulatory requirements for medical devices in that jurisdiction.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue447

Newest first, rows 1-50 of 447

Search and filter all 447 devices
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  • Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • PULLUP Pin Set

    Listed Registry: GUDID Class:I
  • LIGAFIX / PULLUP Pin Set

    Listed Registry: GUDID Class:I
  • LIGAFIX / PULLUP Pin Set

    Listed Registry: GUDID Class:I
  • LIGAFIX Pin Set

    Listed Registry: GUDID Class:I
  • LIGAFIX Pin Set

    Listed Registry: GUDID Class:I
  • BTLOOP Pin Set

    Listed Registry: GUDID Class:I
  • PULLUP Pin Set

    Listed Registry: GUDID Class:I
  • ComposiTCP 30 flat head

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • BIOSORB BIO1 Granules Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • BIOSORB BIO1 Cubes Open recall

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Listed Registry: GUDID Class:I
  • Listed Registry: GUDID Class:I
  • LIGAFIX Chondral pick

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • LIGAFIX 60 round head

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Neotis 50

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Pullup

    Listed Registry: GUDID Class:I
  • ComposiTCP 30 round head

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • ComposiTCP 30 round head

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ComposiTCP 30 flat head

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Otis-C Plus

    Active Regimes: 510(k) Registry: GUDID Class:II
  • MBlock Adjustable Loop XL BTB

    Active Regimes: 510(k) Registry: GUDID Class:II
  • BIOSORB BIO1 Stick Open recall

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • BIOSORB BIO1 Stick Open recall

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • LIGAFIX Router bit

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Biosorb Otis 50

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • OTIS-C PLUS Plate - Left

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ecoFIX

    Listed Registry: GUDID Class:I
  • Neotis

    Active Regimes: 510(k) Registry: GUDID Class:II
  • BIOSORB BIO1 Cubes Open recall

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Biosorb Otis

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • LIGAFIX Drill guide

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • Neotis

    Active Regimes: 510(k) Registry: GUDID Class:II
  • BIOSORB - BIO1-S BIO1-S with Ø 1 mm granules

    Active Regimes: 510(k) Registry: GUDID Class:II
  • ecoFIX

    Withdrawn Registry: GUDID Class:I
  • BIO1-Kit

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Neotis Xs

    Active Regimes: 510(k) Registry: GUDID Class:II
  • LIGAFIX Super elastic guide pin X1

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • LIGAFIX 60 round head

    Active Regimes: 510(k) Registry: GUDID Class:II
  • OTIS metallic trial implant

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:I
  • Otis-C Plus

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Bt Loop

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • ComposiTCP 30 flat head

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • BIOSORB BIO1 Cylinder Open recall

    Active Regimes: 510(k) Registry: GUDID Class:II
  • Neotis

    Active Regimes: 510(k) Registry: GUDID Class:II
  • OTIS Hammer

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • BIOSORB BIO1 Stick Open recall

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • Biosorb Otis 50

    Active Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID Class:II
  • RIGIDLOOP Multilig Adjustable Cortical Button

    Active Regimes: 510(k) Registry: GUDID Class:II

Rows 1-50 of 447

Showing 1-50 of 447

Company details

DUNS number
772462123
Phone
901-203-3470

Frequently asked questions

How many devices does S.B.M have in the registry?

The registry currently lists 447 devices for S.B.M. Devices recorded under merged duplicate company entries are counted once.

Which registries list S.B.M's devices?

Among its 50 most recently registered devices, S.B.M has devices listed in EUDAMED (20 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do S.B.M's devices fall under?

Among its 50 most recently registered devices, the classes recorded for S.B.M's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from S.B.M in the registry?

The most recently registered devices listed for S.B.M include PULLUP Reusable suture retriever pin x10, PULLUP Reusable suture retriever pin x5, PULLUP Pin Set and LIGAFIX / PULLUP Pin Set.

Generated automatically from registry data and not verified by a human reviewer.