Alba-Waldensian, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Albahealth C.A.L.M. Sleeve, Model 59001 Ref K020592
Regimes: 510(k) Registry: 510(k)Compression Devices, Limb Ref K781964
Regimes: 510(k) Registry: 510(k)Sterile Orthopedic Stockinette Ref K780547
Regimes: 510(k) Registry: 510(k)Sterile Impervious Orthopedic Stockin Ref K792357
Regimes: 510(k) Registry: 510(k)Tubular Dressing Retainer Ref K780570
Regimes: 510(k) Registry: 510(k)Heel/Elbow Protector Ref K771913
Regimes: 510(k) Registry: 510(k)Alba Health Pas Wrap System Ref K961405
Regimes: 510(k) Registry: 510(k)Alba Dry Burn Pad Ref K852091
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alba-Waldensian, Inc. have in the registry?
The registry currently lists 8 devices for Alba-Waldensian, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alba-Waldensian, Inc.'s devices?
Among its 8 most recently registered devices, Alba-Waldensian, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Alba-Waldensian, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Alba-Waldensian, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alba-Waldensian, Inc. in the registry?
The most recently registered devices listed for Alba-Waldensian, Inc. include ALBAHEALTH C.A.L.M. SLEEVE, MODEL 59001, COMPRESSION DEVICES, LIMB, STERILE ORTHOPEDIC STOCKINETTE and STERILE IMPERVIOUS ORTHOPEDIC STOCKIN.