ClearanceBrief
Company ยท US

G.W.B. Intl., Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1996. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LZUPlug, Punctum3
OKSLacrimal Stents And Intubation Sets3
HPZImplant, Eye Sphere1
IYOSystem, Imaging, Pulsed Echo, Ultrasonic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 6, 1996K955671RITLENG BICAN.LACR.SETS/SELF THREAD. MONOKAS(CHG.IN STER.)
G.W.B. Intl., Ltd.
OKS
Oct 5, 1995K954094OPHTA SIL- PUNCTAL PLUGS (MODIFICATION)
G.W.B. Intl., Ltd.
LZU
Mar 14, 1995K950569OPHTA SIL {SELF-THREADING MONOKA (RITLENG TYPE)}
G.W.B. Intl., Ltd.
LZU
May 4, 1994K940508OPHTA SIL (RITLENG PROBE AND LACRIMAL INTUBATION SET)
G.W.B. Intl., Ltd.
OKS
Jun 18, 1991K911110OPHTA SIL(R), ENULCEATION/EVISCERATION IMPLANTS
G.W.B. Intl., Ltd.
HPZ
May 13, 1991K911108OPHTA SIL (R), PUNCTAL PLUGS AND INSERTERS
G.W.B. Intl., Ltd.
LZU
May 1, 1991K911109OPHTA SIL (R), LACHRYMAL INTUBATION SETS
G.W.B. Intl., Ltd.
OKS
Jan 12, 1990K896029DIGITAL ULTRASOUND IMAGING SYSTEM DUB 20
G.W.B. Intl., Ltd.
IYO

Latest recalls

DateFirm and productCodeLinked 510(k)
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