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Synergetics, Inc.

Last updated September 17, 2026

Information

Country: US
Address: 3845 Corporate Centre Dr, O Fallon, MO, 63368
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1000119053
DUNS Number: —

Catalogue (580)

Page 10 of 12

Device	Model / Reference	Registries	Class	Status
Synergetics	18064	FDA UDI	Class I	Unknown
Synergetics	39.03.25PIN	FDA UDI	Class I	Active
Synergetics	23.23	FDA UDI	Class I	Active
Synergetics	09.10.23PIN-M	FDA UDI	Class I	Active
Synergetics	09.05.25PIN	FDA UDI	Class I	Active
Synergetics	14.01	FDA UDI	Class I	Active
Codman	80-1274	FDA UDI	Class II	Active
Synergetics	BL5823D	FDA UDI	Class II	Active
Codman	80-7606	FDA UDI	Class II	Active
Synergetics	55.23	FDA UDI	Class II	Active
Synergetics	12.12	FDA UDI	Class I	Active
Synergetics	09.05PIN	FDA UDI	Class I	Active
Synergetics	65027E	FDA UDI	Class II	Active
Synergetics	39.08PIN	FDA UDI	Class I	Active
Synergetics	09.26	FDA UDI	Class I	Active
Synergetics	D30.10.23	FDA UDI	Class I	Active
Synergetics	19020	FDA UDI	Class I	Active
Synergetics	23.56S	FDA UDI	Class I	Active
Synergetics	BL5240	FDA UDI	Class I	Active
Synergetics	23.26.25	FDA UDI	Class I	Active
Synergetics	11.21	FDA UDI	Class I	Active
Synergetics	12.06.27	FDA UDI	Class I	Active
Synergetics	34.77	FDA UDI	Class I	Active
Synergetics	70027S	FDA UDI	Class II	Active
Synergetics	09.50.20	FDA UDI	Class I	Active
Synergetics	39.23.25	FDA UDI	Class I	Active
Synergetics	56.65.25	FDA UDI	Class II	Active
Synergetics	31.00	FDA UDI	Class I	Active
Synergetics	11.06A	FDA UDI	Class I	Active
Synergetics	70127B	FDA UDI	Class II	Active
Synergetics	56.50.29P	FDA UDI	Class II	Active
Synergetics	39.28.25	FDA UDI	Class I	Active
Synergetics	09.10.23A	FDA UDI	Class I	Active
Synergetics	11.01A	FDA UDI	Class I	Active
Synergetics	65935	FDA UDI	Class II	Active
Synergetics	56.44P	FDA UDI	Class II	Active
VersaVit	VERSAVIT	FDA UDI	Class II	Active
Synergetics	56.30.23P	FDA UDI	Class II	Active
Synergetics	09.07.23A	FDA UDI	Class I	Active
Synergetics	10.24.25PIN	FDA UDI	Class I	Active
Synergetics	23.05A	FDA UDI	Class I	Active
Synergetics	09.25.23S	FDA UDI	Class I	Active
Codman	80-1269	FDA UDI	Class II	Active
Synergetics	29.02.23A	FDA UDI	Class I	Active
Synergetics	20.16.25	FDA UDI	Class I	Active
Synergetics	53.00.23	FDA UDI	Class II	Active
Codman	80-7602	FDA UDI	Class II	Active
Synergetics	D11.60	FDA UDI	Class I	Active
Synergetics	11.06.23PIN	FDA UDI	Class I	Active
Synergetics	20023S	FDA UDI	Class II	Active

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FDA Recalls (37)

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
Jun 12, 2024	Z-2253-2024	—	open, classified	Sterilization certificates could not be validated by the supplier
Jun 12, 2024	Z-2254-2024	—	open, classified	Sterilization certificates could not be validated by the supplier
Jun 12, 2024	Z-2252-2024	—	open, classified	Sterilization certificates could not be validated by the supplier
Jun 12, 2024	Z-2251-2024	—	open, classified	Sterilization certificates could not be validated by the supplier
Aug 11, 2016	Z-0120-2017	—	terminated	Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Aug 11, 2016	Z-0122-2017	—	terminated	Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Aug 11, 2016	Z-0121-2017	—	terminated	Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Aug 11, 2016	Z-0119-2017	—	terminated	Vitrectomy cutters have been found not to be operating within the correct pressure pulse per specification.
Dec 9, 2013	Z-0899-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0883-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0892-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0876-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0877-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0895-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0872-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0875-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0873-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0882-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0896-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0885-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0894-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0880-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0881-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0891-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0886-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0874-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0897-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0898-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0878-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0889-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0888-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0884-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0887-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0890-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0879-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Dec 9, 2013	Z-0893-2014	—	terminated	Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Jul 30, 2013	Z-0051-2014	—	terminated	One lot of 25 gauge Soft-Tip Disposable Cannulas are co-mingled with 23 gauge cannulas; the product is labeled as 25 gauge cannulas.