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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 11 of 12

Device	Model / Reference	Registries	Class	Status
Synergetics	56.30.25P	FDA UDI	Class II	Active
Synergetics	56.24.25P	FDA UDI	Class II	Active
Synergetics	11.07A	FDA UDI	Class I	Active
Synergetics	BL5825F	FDA UDI	Class II	Active
Synergetics	10.24.23	FDA UDI	Class I	Active
Synergetics	34.21	FDA UDI	Class I	Active
Synergetics	12.21PIN	FDA UDI	Class I	Active
Synergetics	20020S	FDA UDI	Class II	Active
Synergetics	21.01A	FDA UDI	Class I	Active
Synergetics	58.20V	FDA UDI	Class I	Active
Synergetics	11.21S	FDA UDI	Class I	Active
Synergetics	55.23.27	FDA UDI	Class II	Active
Synergetics	56.46.23P	FDA UDI	Class II	Active
Synergetics	11.03A	FDA UDI	Class I	Active
Synergetics	56.07.25PS	FDA UDI	Class II	Active
Synergetics	39.15.25PIN-M	FDA UDI	Class I	Active
Synergetics	55.26.23L	FDA UDI	Class II	Active
Synergetics	10.01A	FDA UDI	Class I	Active
Synergetics	34.78	FDA UDI	Class I	Active
Synergetics	23.25S	FDA UDI	Class I	Active
Synergetics	57.27	FDA UDI	Class II	Active
Synergetics	11.24	FDA UDI	Class I	Active
Synergetics	BL5827M	FDA UDI	Class II	Active
Synergetics	09.05.25A	FDA UDI	Class I	Active
Synergetics	55.27	FDA UDI	Class II	Active
Synergetics	56.22.25P	FDA UDI	Class II	Active
Synergetics	70020E	FDA UDI	Class II	Active
Synergetics	09.05.23PIN	FDA UDI	Class I	Active
Synergetics	55.25.23TX	FDA UDI	Class II	Active
Synergetics	SL532FF-5	FDA UDI	Class II	Active
Synergetics	55.48.25P	FDA UDI	Class II	Active
Synergetics	39.08.25PIN	FDA UDI	Class I	Active
Synergetics	56.22P	FDA UDI	Class II	Active
Synergetics	55.26.23	FDA UDI	Class II	Active
Synergetics	56.02.27P	FDA UDI	Class II	Active
Synergetics	PLAMP	FDA UDI	Class II	Active
Synergetics	39.15.23PIN	FDA UDI	Class I	Active
Synergetics	11.04A	FDA UDI	Class I	Active
Codman	80-7614	FDA UDI	Class II	Active
Synergetics	23.29S	FDA UDI	Class I	Active
Synergetics	09.08.25A	FDA UDI	Class I	Active
Synergetics	11.46.25PIN	FDA UDI	Class I	Active
Synergetics	55.36.23E	FDA UDI	Class II	Active
Synergetics	BL5627S	FDA UDI	Class II	Active
Synergetics	28.21	FDA UDI	Class I	Active
Synergetics	12.41	FDA UDI	Class I	Active
Synergetics	30.18.23	FDA UDI	Class I	Active
Synergetics	55.26E	FDA UDI	Class II	Active
Synergetics	39.03.23PIN	FDA UDI	Class I	Active
Synergetics	39.28.25S	FDA UDI	Class I	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.