Deka M.E.L.A. SRL
Active in EUDAMEDItalyfrom SRN EUDAMED FDA SRN IT-MF-000007389
Deka M.E.L.A. SRL is a medical device manufacturer based in Italy, with 116 devices listed in EUDAMED and FDA GUDID (EU Class IIb, IIa and I) as of 14 Nov 2026.
- Devices
- 116
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- EUDAMED 116
- FDA GUDID 4
- Device classes
- EU Class IIb 109
- EU Class IIa 4
- EU Class I 3
- Top EMDN categories
- Identifiers
- EUDAMED SRN IT-MF-000007389
At a glance
EU certificates
2 of 3 in force. 1 certificate has expired.
Market reach
- European Union
- EUDAMED actor, 3 certificates
- United States
- FDA establishment
What Deka M.E.L.A. SRL makes
DEKA M.E.L.A. SRL manufactures multi-modality skin treatment systems, including professional red-light phototherapy units and dermatological/carbon dioxide laser systems for surgical and cosmetic applications. Their portfolio also includes microwave ablation probes, transcutaneous neuromuscular electrical stimulation (TENS) devices for physical therapy, and handheld electric massagers. Surgical diode laser systems and specialized handpieces for laser and stimulation therapies are also part of their offerings.
The company’s devices are classified under EU Medical Device Regulations as Class I, Class II, Class IIa, and Class IIb, with listings in the EU’s eudamed registry and the FDA’s UDI database. The manufacturer is based in Italy.
Catalogue
Search and filter all 116 devicesShowing 1-50 of 116
Company details
- EUDAMED SRN
- IT-MF-000007389
- EU VAT number
- 04190470486
- EUDAMED status
- Active
- EUDAMED registered name
- DEKA M.E.L.A. SRL
- Registered address
- 17, Via Baldanzese, 50041, Calenzano (FI), Italy
- Website
- www.dekalaser.com
- linkedin.com/company/deka-laser
- facebook.com/DEKALaser.Official
- info@deka.it
- Phone
- +39 055 8832884
- PRRC contact
- Paolo Peruzzi
EUDAMED certificates
3 certificates2 valid, 1 expiredMDR 3next expiry 18 May 2031
TÜV SÜD Product Service GmbH 0123 2 certificates
- G15 098416 0015 Active
Quality management system EU MDR
- Issued
- 22 Jun 2026
- Expires
- 20 Sep 2031
- Valid from
- 21 Sep 2026
- G10 098416 0009 Expired
Quality management system EU MDR
- Issued
- 23 Apr 2025
- Expires
- 20 Sep 2026
IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. 0051 1 certificate
- 277/MDR Active
Quality management system EU MDR
- Issued
- 19 May 2026
- Expires
- 18 May 2031
FDA establishments
- Deka M.E.L.A. SRL US
From the company website
DEKA introduces PRISMA, the new technological platform that sets a new standard in advanced aesthetics through a unique multilayer approach. Three proven technologies – Advanced Intense Pulsed Light (IPL), Radio Frequency (RF), and Electro Muscle...
Frequently asked questions
How many devices does DEKA M.E.L.A. SRL have in the registry?
The registry currently lists 116 devices for DEKA M.E.L.A. SRL. Devices recorded under merged duplicate company entries are counted once.
Which registries list DEKA M.E.L.A. SRL's devices?
Among its 50 most recently registered devices, DEKA M.E.L.A. SRL has devices listed in EUDAMED (50 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do DEKA M.E.L.A. SRL's devices fall under?
Among its 50 most recently registered devices, the classes recorded for DEKA M.E.L.A. SRL'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 DEKA M.E.L.A. SRL?
EUDAMED lists 3 certificates for DEKA M.E.L.A. SRL (quality management system) under MDR. 2 are recorded with the status issued. The most recent was issued on 22 Jun 2026.
What are the newest devices from DEKA M.E.L.A. SRL in the registry?
The most recently registered devices listed for DEKA M.E.L.A. SRL include TORO, HiScan V2LR, HiScan DOT + and EasySpot Micromanipulator.
Which FDA establishments are linked to DEKA M.E.L.A. SRL?
1 FDA establishment is linked to DEKA M.E.L.A. SRL in the registry; they are listed on the company page.