LISA Laser Products GmbH
DE-MF-000005036 · Germany · Katlenburg-Lindau
LISA Laser Products GmbH is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 43 |
|---|---|
| Class IIa | 1 |
Most frequent device types declared: 101 503 118, 101 503 188, 101 503 189, 101 503 387, 101 503 514.
Among these devices, 14 are declared sterile, 27 reusable, 43 active.
Devices declared under this manufacturer
- FlexiFib
- FlexiFib 5m
- FlexiFib-SU
- FlexiFib-SU smart connector
- LithoFib
- PercuFib
- RevoLix 120
- RevoLix 200
- RevoLix HTL
- RevoMed
- RevoSoft
- RigiFib-SU smart connector
Showing 12 of 44 declared devices.
Catalogue references include 101 503 188, 101 503 189, 101 503 387, 101 503 514, 101 503 650, 105 402 010.
European nomenclature codes declared: Z12011080, Z12011006, Z12011003,Z12011006.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LISA LASER PRODUCTS GMBH (DE) · FDA 3003168101 |
| Devices in EUDAMED | 44 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 44 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 13.6 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. LISA Laser Products GmbH is registered in the United States but was not found in the Canadian register.