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ALPHA-OMEGA SERVICES, INC.

Last updated September 17, 2026

Information

Country: US
Address: 1282 BIG WOODS-STARK RD., Vinton, LA, 70668
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3003660614
DUNS Number: 060398989

Catalogue (75)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
AOS Implant Needle, Series-17, 15 cm, 14°	NID0001-007	FDA UDI	Class II	Active
AOS Universal Connecting Guide Tubes	SGU0007-015	FDA UDI	Class II	Active
AOS Collar and Large O-Ring	CTG1517-001	FDA UDI	Class II	Unknown
AOS Interstitial Templates, Needles, and Accesories	GVN1517-006	FDA UDI	Class II	Active
AOS Implant Needle, Series-17, 15 cm, 30°	NID0001-008	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accessories	CTG1517-001	FDA UDI	Class II	Active
AOS Implant Tube, Intralumenal	TII0004-001	FDA UDI	Class II	Unknown
AOS Flexiguide Needle	NFW0001-009	FDA UDI	Class II	Unknown
AOS Flexiguide Needle	NFV0001-004	FDA UDI	Class II	Unknown
AOS Implant Needle, Series-17, 20 cm, 45°	NID0001-012	FDA UDI	Class II	Unknown
AOS Interstitial Templates, Needles, and Accesories	NHD0001-005	FDA UDI	Class II	Active
AOS Implant Needle, Series-17, 20 cm, 30°	NID0001-011	FDA UDI	Class II	Unknown
AOS Stainless Steel Needle	NHD0001-002	FDA UDI	Class II	Unknown
AOS Prostate Template, Syed/Neblett/Hedger	TPD0001-015	FDA UDI	Class II	Unknown
AOS Stainless Steel Needle	NHD0001-004	FDA UDI	Class II	Unknown
AOS Flexiguide Needle	NFV0002-004	FDA UDI	Class II	Unknown
AOS Retaining Button (Syed Type), Radiopaque	BRS0045-025	FDA UDI	Class II	Active
AOS Universal Connecting Guide Tubes	SGU0007-020	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accesories	NHD0001-003	FDA UDI	Class II	Active
AOS GYN-3 Template, Syed/Neblett/Hedger	TGD0003-017	FDA UDI	Class II	Unknown
AOS Interstitial Templates, Needles, and Accessories	GVN1517-005	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accesories	TGD0003-017	FDA UDI	Class II	Active
AOS Flexiguide Needle	NFW0001-010	FDA UDI	Class II	Unknown
AOS Implant Tube, Intralumenal	TII0005-001	FDA UDI	Class II	Unknown
AOS Vaginal Guide	GVN1517-006	FDA UDI	Class II	Unknown
AOS Stainless Steel Needle	NHD0001-003	FDA UDI	Class II	Unknown
AOS Rectal Template, Syed/Neblett	TRD0001-017	FDA UDI	Class II	Unknown
AOS Universal Connecting Guide Tubes	SGU0010-020	FDA UDI	Class II	Active
AOS Vaginal Guide	GVN1517-005	FDA UDI	Class II	Unknown
AOS Retaining Button (Syed Type), White Nylon	BRS0045-010	FDA UDI	Class II	Active
AOS Implant Tube, Tongue/Soft Tissue, Puthawala/Syed	TIT0001-004	FDA UDI	Class II	Unknown
AOS Marker Seeds	SMG0242-025	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accesories	GVN1517-007	FDA UDI	Class II	Active
AOS GYN-3 Template, yed/Neblett/Hedger	TGD0003-015	FDA UDI	Class II	Unknown
AOS Extension Adaptor	SAE0001-020	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accesories	NHD0001-002	FDA UDI	Class II	Active
AOS Gold Marker Seeds	SMG0242-025	FDA UDI	Class II	Unknown
AOS Rectal Template, Syed/Neblett/Hedger	TRD0001-015	FDA UDI	Class II	Unknown
AOS Flexiguide Needle	NFV0003-003	FDA UDI	Class II	Unknown
AOS Interstitial Templates, Needles, and Accesories	TPD0001-015	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accesories	TPD0001-017	FDA UDI	Class II	Active
AOS Implant Tube, Breast/Head/Neck, Puthawala/Syed	TIB0001-003	FDA UDI	Class II	Unknown
AOS implant Needle, Series-17, 20 cm, 14°	NID0001-010	FDA UDI	Class II	Unknown
AOS Implant Tube, Intralumenal	TII0002-001	FDA UDI	Class II	Unknown
AOS Stainless Steel Needle	NHD0001-006	FDA UDI	Class II	Unknown
AOS Implant Tube, Breast/Head/Neck, Puthawala/Syed	TIB0001-002	FDA UDI	Class II	Unknown
AOS Implant Needle, Series-17, 15 cm, 45°	NID0001-009	FDA UDI	Class II	Unknown
AOS Interstitial Templates, Needles, and Accesories	NHD0001-004	FDA UDI	Class II	Active
AOS Vaginal Guide	GVN1517-007	FDA UDI	Class II	Unknown
AOS Vaginal Guide	GVN1517-008	FDA UDI	Class II	Unknown

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FDA Recalls (14)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Nov 15, 2007	Z-0169-2009	—	terminated	There is a possibility that the Flexiguide Needle tip is defective. There is the potential for the needles tip to leak, thereby breaking the sterile boundary and possibly contaminating other devices with body fluids.
Nov 15, 2007	Z-0167-2009	—	terminated	There is a possibility that the Flexiguide Needle tip is defective. There is the potential for the needles tip to leak, thereby breaking the sterile boundary and possibly contaminating other devices with body fluids.
Nov 15, 2007	Z-0168-2009	—	terminated	There is a possibility that the Flexiguide Needle tip is defective. There is the potential for the needles tip to leak, thereby breaking the sterile boundary and possibly contaminating other devices with body fluids.
Nov 15, 2007	Z-0170-2009	—	terminated	There is a possibility that the Flexiguide Needle tip is defective. There is the potential for the needles tip to leak, thereby breaking the sterile boundary and possibly contaminating other devices with body fluids.
Nov 15, 2007	Z-0166-2009	—	terminated	There is a possibility that the Flexiguide Needle tip is defective. There is the potential for the needles tip to leak, thereby breaking the sterile boundary and possibly contaminating other devices with body fluids.
Feb 21, 2006	Z-0816-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0820-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0814-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0818-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0817-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0815-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0813-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Feb 21, 2006	Z-0819-06	—	terminated	There is a possibility that the diameter of the catheter does not meet specifications. As a result it may not be possible to correctly connect the catheter to a VariSource Quick Connect. This would prevent any treatment. Furthermore, since the problem would not be apparent until after the catheter has been implanted an unnecessary surgical implantation procedure would have taken place.
Sep 4, 2003	Z-0570-04	—	terminated	Template needle may fracture leaving tip in patient.