Aesculap-Meditec GmbH
Country not established
- Devices
- 3
What Aesculap-Meditec GmbH makes
Aesculap-Meditec GmbH manufactures laser systems for dermatological and ophthalmic procedures, including YAG lasers for eye surgery and erbium and CO₂ lasers for skin resurfacing and tissue ablation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Phacolase Er: Yag Laser Ref K991993
Regimes: 510(k) Registry: 510(k)Mcl 29 Dermablate Erbium Laser System Ref K964128
Regimes: 510(k) Registry: 510(k)Multipulse CO2 Laser Ref K983215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aesculap-Meditec GmbH have in the registry?
The registry currently lists 3 devices for Aesculap-Meditec GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aesculap-Meditec GmbH's devices?
Among its 3 most recently registered devices, Aesculap-Meditec GmbH has devices listed in FDA 510(k) (3 devices).
What risk classes do Aesculap-Meditec GmbH's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Aesculap-Meditec GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aesculap-Meditec GmbH in the registry?
The most recently registered devices listed for Aesculap-Meditec GmbH include PHACOLASE ER: YAG LASER, MCL 29 DERMABLATE ERBIUM LASER SYSTEM and MULTIPULSE CO2 LASER.