G.W.B. Intl., Ltd.
Country not established
- Devices
- 8
What G.W.B. Intl., Ltd. makes
G.W.B. Intl., Ltd. manufactures ophthalmic devices including punctal plugs and inserters, lacrimal intubation sets, self-threading monoka probes, enucleation and evisceration implants, and digital ultrasound imaging systems such as the DUB 20.
The company's devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the manufacturer is based in the United States.
Catalogue
Ophta Sil (R), Punctal Plugs And Inserters Ref K911108
510(k) 510(k)Digital Ultrasound Imaging System Dub 20 Ref K896029
510(k) 510(k)Ophta Sil {self-Threading Monoka (Ritleng Type)} Ref K950569
510(k) 510(k)Ophta Sil (R), Lachrymal Intubation Sets Ref K911109
510(k) 510(k)- 510(k) 510(k)
Ophta Sil(R), Enulceation/Evisceration Implants Ref K911110
510(k) 510(k)- 510(k) 510(k)
Ophta Sil- Punctal Plugs (Modification) Ref K954094
510(k) 510(k)
Frequently asked questions
How many devices does G.W.B. Intl., Ltd. have in the registry?
The registry currently lists 8 devices for G.W.B. Intl., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list G.W.B. Intl., Ltd.'s devices?
Among its 8 most recently registered devices, G.W.B. Intl., Ltd. has devices listed in FDA 510(k) (8 devices).
What risk classes do G.W.B. Intl., Ltd.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for G.W.B. Intl., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from G.W.B. Intl., Ltd. in the registry?
The most recently registered devices listed for G.W.B. Intl., Ltd. include OPHTA SIL (R), PUNCTAL PLUGS AND INSERTERS, DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20, OPHTA SIL {SELF-THREADING MONOKA (RITLENG TYPE)} and OPHTA SIL (R), LACHRYMAL INTUBATION SETS.