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Neoss AB

Active in EUDAMED

Swedenfrom SRN EUDAMED FDA SRN SE-MF-000022321 FEI 3017399129

Neoss AB is a medical device manufacturer based in Sweden, with 543 devices listed in FDA GUDID and EUDAMED (FDA Class II and I; EU Class IIa and I) as of 12 Nov 2026.

Devices
543
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 475
  • EUDAMED 209

A device listed in two registries counts in both.

Device classes
  • FDA Class II 351
  • FDA Class I 115
  • EU Class IIa 48
  • EU Class I 29
Top EMDN categories
Identifiers
  • EUDAMED SRN SE-MF-000022321
  • FDA FEI 3017399129
  • DUNS 509583543

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA establishment

Catalogue543

Newest first, rows 1-50 of 543

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Rows 1-50 of 543

Showing 1-50 of 543

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
SE-MF-000022321
FDA FEI number
3017399129
DUNS number
509583543
EU VAT number
SE556683545901
EUDAMED status
Active
EUDAMED registered name
Neoss AB
Registered address
20, Arvid Wallgrens Backe, 413 46, Göteborg, Sweden
Phone
866 626 3677
PRRC contact
Maria Lopez(public in EUDAMED)

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Neoss, Ltd. US

Frequently asked questions

How many devices does Neoss AB have in the registry?

The registry currently lists 543 devices for Neoss AB. Devices recorded under merged duplicate company entries are counted once.

Which registries list Neoss AB's devices?

Among its 50 most recently registered devices, Neoss AB has devices listed in EUDAMED (50 devices).

What risk classes do Neoss AB's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Neoss AB's devices are Class I and Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Neoss AB in the registry?

The most recently registered devices listed for Neoss AB include Neoss® Guide - Countersink, Ø5.0 S - Wide G5, Neoss® Guide - Countersink, Ø3.5 S/T/E - Narrow G3/5/7, Neoss® Guide - Twist Drill, Tapered ∅3.0 × 7-15 mm and Neoss® Guide - Implant Mount SP, Wide G5.

Which FDA establishments are linked to Neoss AB?

1 FDA establishment is linked to Neoss AB in the registry; they are listed on the company page.

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