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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: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3003660614
DUNS Number: 060398989

Catalogue (75)

Page 2 of 2

Device	Model / Reference	Registries	Class	Status
AOS Prostate Template, Syed/Neblett/Hedger	TPD0001-017	FDA UDI	Class II	Unknown
AOS Implant Tube, Tongue/Soft Tissue, Puthawala/Syed	TIT0001-005	FDA UDI	Class II	Unknown
AOS Interstitial Templates, Needles, and Accesories	GVN1517-008	FDA UDI	Class II	Active
AOS Interstitial Templates, Needles, and Accesories	TGD0003-015	FDA UDI	Class II	Active
AOS Flexiguide Needle	NFV0002-002	FDA UDI	Class II	Unknown
AOS Stainless Steel Needle	NHD0001-005	FDA UDI	Class II	Unknown
AOS Implant Tube, Intralumenal	TII0002-002	FDA UDI	Class II	Unknown
AOS Flexiguide Needle	NFV0001-003	FDA UDI	Class II	Unknown
AOS Universal Connecting Guide Tubes	SGU0010-015	FDA UDI	Class II	Active
AOS Retaining Button, Stainless Steel	BRS0045-008	FDA UDI	Class II	Active
AOS Extension Adaptor	SAE0001-015	FDA UDI	Class II	Active
AOS Flexiguide Needle	NFV0002-003	FDA UDI	Class II	Unknown
AOS Retaining Button (Syed Type), Green Nylon	BRS0045-001	FDA UDI	Class II	Active
AOS Implant Tube, Intralumenal	TII0005-006	FDA UDI	Class II	Unknown
AOS Implant Tube, Intralumenal	TII0005-011	FDA UDI	Class II	Unknown
AOS Implant Tube	TIS0002-002	FDA UDI	Class II	Unknown
Aos Orion Ir-192 Source Cable	K102811	FDA 510(k)	Class II	Active
Aos Universal Conecting Guide Tube	K062824	FDA 510(k)	Class II	Active
Aos Implant Tubes, Implant Needles & Retaining Bottons	K062826	FDA 510(k)	Class II	Active
Aos Marker Seeds	K062825	FDA 510(k)	Class II	Active
AOS Marker Seeds (SMG0242-025)	K233626	FDA 510(k)	Class II	Active
10 Curie Irdium 192, Csn00100-192	K991571	FDA 510(k)	Class II	Active
Aos Interstitial Templates, Needles & Accessories	K062823	FDA 510(k)	Class II	Active
AOS Interstitial Templates, Needles, and Accessories	K233628	FDA 510(k)	Class II	Active
Aos Universal Connecting Guide Tube For High Dose Rate Afterloaders	K964910	FDA 510(k)	Class II	Active

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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.