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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 6 of 12

Device	Model / Reference	Registries	Class	Status
Synergetics	20.41.23	FDA UDI	Class I	Active
Synergetics	23.06.25A	FDA UDI	Class I	Active
Synergetics	56.02	FDA UDI	Class II	Active
Synergetics	70125B	FDA UDI	Class II	Active
Synergetics	D39.10.23	FDA UDI	Class I	Active
Synergetics	23.06.23A	FDA UDI	Class I	Active
Synergetics	55.62.25PX	FDA UDI	Class II	Active
Synergetics	DSYN-LB90-15I	FDA UDI	Class II	Active
Synergetics	11.22S	FDA UDI	Class I	Active
Photon	PHOTON-2X	FDA UDI	Class II	Active
Synergetics	39.12.23PIN	FDA UDI	Class I	Active
Synergetics	11.04.23PIN	FDA UDI	Class I	Active
Synergetics	57.30	FDA UDI	Class II	Active
Synergetics	55.231	FDA UDI	Class II	Active
Synergetics	65933	FDA UDI	Class II	Active
Synergetics	20.30	FDA UDI	Class I	Active
Synergetics	57.26	FDA UDI	Class II	Active
Synergetics	55.69.25P	FDA UDI	Class II	Active
Codman	80-1272	FDA UDI	Class II	Active
Synergetics	58.00.23	FDA UDI	Class I	Active
Synergetics	20.16.23	FDA UDI	Class I	Active
Synergetics	58.25STHV	FDA UDI	Class I	Active
Synergetics	56.21.27P	FDA UDI	Class II	Active
Synergetics	23.28S	FDA UDI	Class I	Active
Synergetics	BL5623S	FDA UDI	Class II	Active
Synergetics	39.24S	FDA UDI	Class I	Active
Synergetics	10.24.25	FDA UDI	Class I	Active
Synergetics	09.25	FDA UDI	Class I	Active
Photon	PHOTON-1X	FDA UDI	Class II	Active
Synergetics	VVITFPEDAL-A	FDA UDI	Class II	Active
Synergetics	56.30	FDA UDI	Class II	Active
Synergetics	55.25.23	FDA UDI	Class II	Active
Synergetics	55.23.25	FDA UDI	Class II	Active
Synergetics	08.01	FDA UDI	Class I	Active
Codman	80-1275	FDA UDI	Class II	Active
Synergetics	58.25SV	FDA UDI	Class I	Active
Synergetics	53.00.27	FDA UDI	Class II	Active
Synergetics	20.18	FDA UDI	Class I	Active
Synergetics	57.31	FDA UDI	Class II	Active
Codman	80-7611	FDA UDI	Class II	Active
Synergetics	23.25	FDA UDI	Class I	Active
Synergetics	09.26S	FDA UDI	Class I	Active
Synergetics	30.32.23	FDA UDI	Class I	Active
Synergetics	58.00.20	FDA UDI	Class I	Active
Synergetics	09.12.23PIN	FDA UDI	Class I	Active
Synergetics	12.06.25	FDA UDI	Class I	Active
Synergetics	30.80.25	FDA UDI	Class I	Active
Synergetics	55.36.251E	FDA UDI	Class II	Active
Synergetics	56.14	FDA UDI	Class II	Active
Synergetics	55.21.231	FDA UDI	Class II	Active

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Importers

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Authorities

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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.