KLS Martin SE & Co. KG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000005551 FEI 3036795921
- Devices
- 8,108
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
3 of 3 in force.
Market reach
- European Union
- EUDAMED actor, 3 certificates
- United States
- FDA FEI
What KLS Martin SE & Co. KG makes
KLS Martin SE & Co. KG manufactures surgical instruments and medical devices, including the MedLED Spectra bezel-only unit, which is designed for surgical lighting applications. The portfolio covers a range of reusable and single-use tools for orthopedic, trauma, and general surgery procedures.
The company’s devices are classified under EU regulations as Class I and Class IIb, with listings maintained in the EU’s eudamed registry. The manufacturer is based in Germany.
Catalogue
Search and filter all 8,108 devicesShowing 1-50 of 8,108
Company details
- EUDAMED SRN
- DE-MF-000005551
- FDA FEI number
- 3036795921
- EU VAT number
- DE 142930777
- EUDAMED status
- Active
- EUDAMED registered name
- KLS Martin SE & Co. KG
- Registered address
- 1, KLS Martin Platz, 78532, Tuttlingen, Germany
- Website
- www.klsmartin.com
- de-de.facebook.com/klsmartin
- [email protected]
- Phone
- +49 7461 706 0
- PRRC contact
- Ingo Leukart
EUDAMED certificates
3 certificates3 valid, 0 expiredMDR 3next expiry 15 Oct 2029
DNV MEDCERT GmbH 0482 3 certificates
- 20452GB450250508 Active
Technical documentation EU MDR
- Issued
- 8 May 2025
- Expires
- 7 May 2030
- 20487GB450260901 Active
Technical documentation EU MDR
- Issued
- 1 Sep 2026
- Expires
- 24 Apr 2030
- Reason
- Add device or group
- 20486GB450260713 Active
Technical documentation EU MDR
- Issued
- 13 Jul 2026
- Expires
- 15 Oct 2029
- Reason
- Add device or group
From the company website
Die KLS Martin Group ist eine international agierende Unternehmensgruppe für innovative Medizintechnik in fast allen Bereichen der Chirurgie.
Frequently asked questions
How many devices does KLS Martin SE & Co. KG have in the registry?
The registry currently lists 8108 devices for KLS Martin SE & Co. KG. Devices recorded under merged duplicate company entries are counted once.
Which registries list KLS Martin SE & Co. KG's devices?
Among its 50 most recently registered devices, KLS Martin SE & Co. KG has devices listed in EUDAMED (50 devices).
What risk classes do KLS Martin SE & Co. KG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for KLS Martin SE & Co. KG's devices are Class I, Class IIa and Class IIb. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for KLS Martin SE & Co. KG?
EUDAMED lists 3 certificates for KLS Martin SE & Co. KG (technical documentation) under MDR. 1 is recorded with the status issued. The most recent was issued on 1 Sep 2026.
What are the newest devices from KLS Martin SE & Co. KG in the registry?
The most recently registered devices listed for KLS Martin SE & Co. KG include KLS Martin.